Zimmer, Inc.,
Medimpex United, Inc.,
Herger AG,
more...
Cervical specula consists of tubes or bi-valve instruments, mounted on shanks, or handles, of sufficient length to admit of introduction through or by means of a vaginal speculum. They are little employed except as a shield to prevent instrumental injury to the cervix, or misapplication of caustics intended for points within the fundus. Vaginal specula are used to spread, retract or dilate the vagina, either for purposes of examination or for treatment. It is also used for anal surgery, although several other forms of anal specula exist. One common form, the sigmoidoscope, resembles a tube that has a removable bullet shaped insert. When the speculum is inserted into the rectum, the insert dilates the rectum to the diameter of the tube. The insert is then removed, leaving the tube to allow examination of the rectum.
High Class Dental,
Heine USA Ltd.,
Cirrus Healthcare Products, L.L.C.,
more...
Conkin Surgical Instruments Ltd.
Rhein Medical Inc.,
Elmed Inc.,
Zimmer, Inc.,
more...
(FDA Code:
NJC /
878.43)
Identification. An implantable clip is a clip-like device intended to connect internal tissues to aid healing. It is not absorbable.
Classification. Class II.
Gyrx, LLC
A vascular catheter contains a catheter body, which is made up of an inner tube formed of a metal or an alloy, and an outer tube formed of a synthetic resin covering the outside surface of the inner tube. The inner tube has one or more spiral slits in the distal end portion. A vascular dilatation instrument includes an inner tube, an outer tube disposed coaxially around the inner tube, and an inflatable member having one end attached to the inner tube and another end attached to the outer tube.
Bacchus Vascular,
MRI Medical,
Medcomp,
more...
Vascular lesion removal lasers are used to remove the vascular lesions present in the skin. Problems such as tiny blood vessels that develop from sun exposure, hemangiomas or conditions like rosacea (an entity partly characterized by blood vessels) can be improved or eradicated without scarring. Medical conditions that were once impossible to treat, such as port-wine stain hemangiomas, which are flat vascular patches present since birth, may now be substantially improved or even completely eliminated. Blood vessels of the legs, sometimes known as spider veins, can also be greatly improved or even made to disappear. The laser treats very small blood vessels most effectively and dermatologic conditions improved by the vascular laser include scars and stretch marks. Reddish, elevated, and itchy scars can be made less red, flatter, and less bothersome by treatment with the proper laser. Thay can be appropriately used for the soles of the feet, where recalcitrant warts can occur.
Lumenis Inc.,
Cynosure, Inc,
Medart Corp.,
more...
Wholesales Surgical Instruments, Inc.,
Southpointe Surgical Supply, Inc.,
Rhein Medical Inc.,
more...
(FDA Code:
NJZ /
878.48)
Identification. A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9.
Marina Medical Instruments Inc.,
Vustik, Inc.,
Bio-Bridge Science, Inc.,
more...
U.S.E Surgical Instruments,
Germed USA Inc.,
Boss Instruments, Ltd.,
more...
Terumo Cardiovascular Systems,
Cathex Co., Ltd,
Sanxin Medical Devices Group
Cardinal Health, Inc.
Codman & Shurtleff, Inc.
Cloward Instruments Corporation,
Codman & Shurtleff, Inc.,
Millennium Surgical Corp.
Codman & Shurtleff, Inc.,
Medtronic, Inc.,
Repro-Med Systems, Inc.,
more...
(FDA Code:
FKA /
876.554)
Identification. A blood access device and accessories is a device intended to provide access to a patient's blood for hemodialysis or other chronic uses. When used in hemodialysis, it is part of an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and provides access to a patient's blood for hemodialysis. The device includes implanted blood access devices, nonimplanted blood access devices, and accessories for both the implanted and nonimplanted blood access devices.
Classification. (1) Class III (premarket approval) for the implanted blood access device.
Millennium Surgical Corp.,
Synovis Micro Companies Alliance Inc,
C. R. Bard, Inc., Bard Medical Div.,
more...
Vicryl suture is a synthetic absorbable sterile surgical suture composed of a copolymer made from 90% glycolide and 10% L-lactide. It is used in general soft tissue approximation and ligation including the ophthalmic procedures.
W. l. Gore & Associates, Inc.,
Ethicon, Inc.,
Medstar, LLC,
more...
Autosuture,
Ethicon, Inc.,
Medstar, LLC,
more...
Cambrian Medical Inc.
Medical Supplies & Equipment Company LLC,
Latam Medical
Adept-Med International, Inc.
AZReam, Inc.,
Solaris-Newtech, Inc.,
Dealmed Medical Supplies,
more...
Vital sign monitor feature large color LEDs for numeric display, high resolution LCD for tabular trends & SpO2 waveform display, adjustable audible & visual alarms and central station networking. Vital sign monitors are used for measuring ECG readings, respiration, temperature and oximetry. It is designed for the 60+ groups.
OBGYN Solution,
AZReam, Inc.,
Southern California Surgical,
more...
AZReam, Inc.,
Nihon Kohden America, Inc.,
A&D Medical,
more...
MedPACS Display, Inc.
Volumetric Infusion Pump is a medical device that delivers intravenous fluids and medicine to patients in hospitals, outpatient surgical centers, hospices, nursing homes and in ambulances. It is used throughout the hospital, including in the emergency room, the I.C.U. and in pediatric units.
Byron Medical, Inc.,
Medtronic MiniMed, Inc.,
Spectrum Laboratories, Inc.,
more...
(FDA Code:
GCX /
880.674)
Identification. A vacuum-powered body fluid suction apparatus is a device used to aspirate, remove, or sample body fluids. The device is powered by an external source of vacuum. This generic type of device includes vacuum regulators, vacuum collection bottles, suction catheters and tips, connecting flexible aspirating tubes, rigid suction tips, specimen traps, noninvasive tubing, and suction regulators (with gauge).
Classification. Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to 880.9.
Byron Medical, Inc.,
Autosuture,
Cooper Surgical, Inc.,
more...
Spectrum Laboratories, Inc.,
Unipack Medical Corporation,
CWI Medical, LLC,
more...
Elantec Medical, Inc.
E.A.R. Inc. / Insta-Mold West,
Gillen Industries
SBH Surgical,
Millennium Surgical Corp.,
Buxton Biomedical, Inc.,
more...
Alba Healthcare,
Nutramax Products, Inc.,
Covidien,
more...
Cutera, Inc.,
Nidek Inc.,
Intralase Corporation,
more...
Comfort Safety Products, Inc.,
Dealmed Medical Supplies,
Kronring HB
Wound is a break in the skin. It is usually caused by cuts or scrapes. Different kinds of wounds may be treated differently from one another, depending upon how they happened and how serious they are.
Medical Distribution Network,
Sunrise Medical,
Action Bandage L.L.C.,
more...
MedicalSupply123.com,
Medical Distribution Network,
Purity Medical Products,
more...
Roboz Surgical Instrument Co., Inc.,
Codman & Shurtleff, Inc.,
Mikron Precision, Inc.,
more...
(FDA Code:
MGO /
878.4018)
Autosuture,
Halyard Health, Inc.,
KitoTech Medical, Inc.,
more...
Wound closure system contains skin closure and a transparent dressing. It is useful for post-endoscopic applications and other sites for additional protection against wetting and peeling.
AZReam, Inc.,
Senvok.com,
Covidien,
more...
Senvok.com,
Halo Medical International
AZReam, Inc.,
American Environmental Health & Safety,
Tellus Medical Products, Inc.,
more...
(FDA Code:
MCY /
880.5075)
Hologic Inc,
Haemonetics Corporation,
3M Medical Specialties,
more...
(FDA Code:
NYS /
878.4015)
Quick-Med Technologies, Inc.,
Derma Sciences, Inc.
Hayes Medical, Inc.,
Spectrum Laboratories, Inc.,
KCK Medical,
more...
(FDA Code:
KOZ /
878.4018)
Identification. A hydrophilic wound dressing is a sterile or non-sterile device intended to cover a wound and to absorb exudate. It consists of nonresorbable materials with hydrophilic properties that are capable of absorbing exudate (e.g., cotton, cotton derivatives, alginates, dextran, and rayon). This classification does not include a hydrophilic wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in part 807, subpart E of this chapter subject to the limitations in 878.9.
Integra LifeSciences Corporation,
Ethicon, Inc.,
Marine Medical International,
more...
Omega Laser Systems Ltd.,
Center Of Laser Technology,
Dr.Suwelack Skin & Health Care Ag,
more...
Wound skin closure stacking rack and tray is a stacking rack for organizing and storing a variety of skin closure product styles and sizes.
Southpointe Surgical Supply, Inc.,
High Class Dental,
MediSource Inc.,
more...
(FDA Code:
GDY /
878.445)
Identification. Nonabsorbable gauze for internal use is a device made of an open mesh fabric intended to be used inside the body or a surgical incision or applied to internal organs or structures, to control bleeding, absorb fluid, or protect organs or structures from abrasion, drying, or contamination. The device is woven from material made of not less than 50 percent by mass cotton, cellulose, or a simple chemical derivative of cellulose, and contains x-ray detectable elements.
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in 878.9.
Lifescience Plus, Inc.,
Ultracell Medical Technologies, Inc.,
Autosuture,
more...
Ultracell Medical Technologies, Inc.,
Codman & Shurtleff, Inc.,
RF Care Systems, LLC,
more...
(FDA Code:
GCT /
876.15)
Identification. An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
Classification. (1) Class II (performance standards).
Elmed Inc.,
Vyaire Medical, Inc.,
Luxtec,
more...