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Sterile ENT Piston Cutting Jig Suppliers

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 EMAIL INQUIRY to  9 suppliers  
Medtronic Xomed Surgical Products, Inc | Address: 6743 Southpoint Drive North, Jacksonville, Florida 32216-0980, USA USA
www.xomed.com | Phone: +1-(904)-296-9600, 800-874-5797
FDA Registration: 1045254  Year Established: 1999  Annual Revenues: USD 500 Million to 1 Billion  Employee Count: ~650  Quality: ISO 9001, CE Certified
Products: Sinus Trochars and Cannulae, Surgical Navigation Interface/Display, Nerve Stimulators, Eyeshields, General Diagnostic Supplies, General Surgical Aids, ...
Medtronic Xomed Surgical Products, Inc develops products that treat people with ear, nose and throat (ENT) diseases. our products include MeroPack®, Bioresorbable Nasal Dressing and Sinus Stent, I more...
 
Bausch & Lomb | Address: 1400 N. Goodman St., Rochester, New York 14609, USA USA
www.bausch.com | Send Inquiry | Phone: +1-(585)-338-6000, 800-553-5340
FDA Registration: 1920664  Annual Revenues: USD 100-500 Million  Employee Count: ~1000  Quality: ISO 9000, ISO 9001, ISO 9002, CE Certified
Products: Daily Wear Soft Contact Lenses (FDA Code: LPL), Extended Wear Soft Contact Lenses (FDA Code: LPM), Soft Contact Lense Rinsing Solutions, Soft Contact Lens Storage Solutions, Contact Lens Eye Drops, Soft Contact Lenses For Extended Wear, ...
Bausch & Lomb is the eye health company dedicated to perfecting vision and enhancing life. We offer a comprehensive portfolio of eye health products. Our three broad categories of products are vision more...
Smith & Nephew Inc. | Address: 1450 Brooks Road, Memphis, Tennessee 38116, USA USA
www.smith-nephew.com | Phone: +1-(901)-399-2121, 800-821-5700
Annual Revenues: USD 50-100 Million  Employee Count: ~400  Quality: ISO 9001 Certified
Products: Middle Ear Implants, ENT Implants, Ventilation Tubes, AC-Powered Operating Room Table (FDA Code: FQO), AC-Powered Surgical Instrument Motor (FDA Code: GEY), AC-Powered Motor Orthopedic Surgical Instrument (FDA Code: HWE), Abdominal Trocar, ...
Smith & Nephew is a wound care management company that manufactures and supplies medical products for the diagnosis of wound care management. Our products & services for wound, skin, IV, & burn care i more...
Gyrus ENT | Address: 2925 Appling Rd, Bartlett, Tennessee 38133, USA USA
www.retroxhearing.com | Phone: +1-(800)-2623540
FDA Registration: 1037007
Products: Video Otoscopes, Digital Hearing Aids, Surgical Cochlear Implant (FDA Code: MCM), BTE Hearing Aids, Canal Hearing Aids, Industrial, & Specialty Cases, ...
Gyrus ENT deals with otology, sinus and rhinology fields. We offer otology implants, microsurgical instruments, powered dissectors and biomaterials for sinus surgery. Our retrox, a hearing system is d more...
Osung Industrial Co. | Address: 324, Kunha-Ri, Wolgod-Myeon, Kimpo-Kun, Kyungki-Do 415-870, Korea, Republic Of Korea, Republic Of
Phone: +82-(31)-987-5395
FDA Registration: 9616119
Products: Anesthesia Conduction Kit (FDA Code: CAZ), Portable Air Compressor (FDA Code: BTI), Labeled Medical Laboratory Equipment (FDA Code: LXG), General Medical Device, Percussor, Vibrator (FDA Code: GWZ), Sterile ENT Piston Cutting Jig (FDA Code: JXY), ...
Osung Industrial Co. offers folding aspirating syringes. more...
Olympus Imaging Corporation | Address: 3-1 Nishi-Shinjuku 2-chome, Shinjuku-ku, Tokyo 163-0914, Japan
www.olympus.co.jp | Phone: +81-(3)-3340-2111
FDA Registration: 8010047
Products: Flexible Endoscope Accessory Hanger, Flexible Endoscopes (FDA Code: GCQ), Flexible Endoscope Repair Parts - Biopsy Channels, Flexible Endoscope Repair Parts - Insertion Tubes, Flexible/Rigid Bronchoscope (FDA Code: EOQ), Non Rigid Laryngoscope (FDA Code: CAL), ...
Olympus Imaging Corporation specializes in medical endoscopes and surgical products,artificial bone replacement material and dental products. We also deal with microscopes and the medical information more...
General Surgical Co., (india) Pvt. Ltd. | Address: G-6 Gee Cee Crescent, 114, Ponamallee High Road, Chennai, Tamil Nadu 60084, India India
www.gescoindia.com | Send Inquiry | Phone: +91-(44)-2825 96 02
FDA Registration: 9613926  Quality: ISO 9001:2000 Certified
Products: Small Depth Gauge (FDA Code: HTJ), Depth Gauge (FDA Code: HTJ), Y-Stent Forceps, Guiding Probes, Flexible Depth Gauge (FDA Code: HTJ), ENT Forceps (FDA Code: KAE), ...
General Surgical Co., (india) Pvt. Ltd. is a manufacturer of surgical instruments. We produce medical & surgical disposables, general, ENT, neuro & spinal, orthopedic, gynecology & obstetrics, plastic more...
Medicon eG | Address: Postfach 44 55, Tuttlingen D-78509, Germany Germany
www.medicon.de | Send Inquiry | Phone: +49-(0)-7462/20-09-0
FDA Registration: 8010099  Employee Count: ~30  Quality: ISO 9001, CE Certified
Products: Clamps, Curettes, Forceps (FDA Code: HTD), Scissors, Titanium Plating Systems, Pituitary Scoops, ...
Medicon eG specializes in the production of surgical tools. We offer a wide range of instruments for anaesthesia. Our modified magill forceps are characterised by atraumatic jaws that render safe and more...
Etablissements Boutmy S.A. | Address: Saint Aubin Le Monial, Rue Le Pavillon, Bourbon L Archambault 03160, France
Phone: +33-(70)-67-0451
FDA Registration: 9680837
Products: Nasal Rasps (FDA Code: KBA), Adjustable Frequency Tuning Fork, Hertz Frequency Tuning Fork, Sensory Evaluation Tuning Fork, Aluminium Tuning Fork, Magnesium Tuning Forks, ...
Etablissements Boutmy S.A. specializes in offering disposable and implantable products. Our products include obstetric and gynecologic general manual instruments, tongue depressor, various needle hold more...
 EMAIL INQUIRY to  9 Sterile ENT Piston Cutting Jig suppliers  
FDA Code / Regulation: JXY / 874.3540

A prosthesis modification instrument for ossicular replacement surgery is a device intended for use by a surgeon to construct ossicular replacements. This generic type of device includes the ear, nose, and throat cutting block; wire crimper, wire bending die; wire closure forceps; piston cutting jib; gelfoamTMpunch; wire cutting scissors; and ossicular finger vise.

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 874.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exception of 820.180 of this chapter, with respect to general requirements concerning records, and 820.198 of this chapter, with respect to complaint files.

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