Boston Medical Products, Inc.

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Contact: Stuart Montgomery - Director of Sales
Web: http://www.bosmed.com
E-Mail:
Address: 117 Flanders Road, Westborough, Massachusetts 01581-1042, USA
Phone: +1-(508)-898-9300, 800-433-2674 | Fax: +1-(508)-898-2373 | Map/Directions >>

Profile: Boston Medical Products, Inc. specializes in ENT surgical & respiratory products. We offer otology, rhinology, laryngeal & esophageal, throplasty, pulmonolgy, and Safe-T-Tubes™ airway management products. Our otology products include Otocell® ear wicks, instrument wipes, silicone strips, Otosilk™ otological strips, graft dressing and doyle ear dressing. We offer many solutions for airway management, including tracheostomy tubes, stoma buttons, speaking valve, and a complete line of accessories. The tracheostomy tube is a flexible tube designed to conform to individual anatomies while providing patient comfort. The Montgomery™ Safe-T-Tube is designed to maintain an adequate airway as well as to provide support in the stenotic trachea that has been reconstructed. This is easy to insert, suck, and remove, and can be used with anesthesia. The laryngeal stent is a molded silicone prosthesis designed to conform to the normal endolaryngeal surface.

The company was founded in 1980, has revenues of USD 1-5 Million, has ~20 employees and is ISO 9001, CE certified.

FDA Registration Number: 1219795

38 Products/Services (Click for related suppliers)

• Bronchoscopy Forceps

• Ear Dressings

• Ear Wick (FDA Code: KCN / 874.5220)

An ear, nose, and throat drug administration device is one of a group of ear, nose, and throat devices intended specifically to administer medicinal substances to treat ear, nose, and throat disorders. These instruments include the powder blower, dropper, ear wick, manual nebulizer pump, and nasal inhaler.

• ENT Esophageal Dilator (FDA Code: KCF / 874.4420)

• ENT Manual Surgical Instrument (FDA Code: LRC / 874.4420)

• ENT Nerve Stimulator (FDA Code: ETN / 874.1820)

A surgical nerve stimulator/locator is a device that is intended to provide electrical stimulation to the body to locate and identify nerves and to test their excitability.

• ENT Synthetic Polyamide Polymer (FDA Code: KHJ / 874.3620)

Ear, nose, and throat synthetic polymer material is a device material that is intended to be implanted for use as a space-occupying substance in the reconstructive surgery of the head and neck. The device is used, for example, in augmentation rhinoplasty and in tissue defect closures in the esophagus. The device is shaped and formed by the suregon to conform to the patient's needs. This generic type of device is made of material such as polyamide mesh or foil and porous polyethylene.

• Epistaxis Balloon (FDA Code: EMX / 874.4100)

An epistaxis balloon is a device consisting of an inflatable balloon intended to control internal nasal bleeding by exerting pressure against the sphenopalatine artery.

• Epistaxis Catheters

• Esophageal Tubes

• External Gauge (FDA Code: GER)

• Instrument Wipe

• Intranasal Septal Splint (FDA Code: LYA / 874.4780)

An intranasal splint is intended to minimize bleeding and edema and to prevent adhesions between the septum and the nasal cavity. It is placed in the nasal cavity after surgery or trauma. The intranasal splint is constructed from plastic, silicone, or absorbent material.

• Laryngeal Keels

• Laryngeal Stents

• Laryngectomy Tube (FDA Code: KAC / 874.4420)

• Larynx Prosthesis (FDA Code: FWN / 874.3620)

• Nasal Septal Button (FDA Code: LFB)

• Nasal Splints (FDA Code: EPP / 874.5800)

An external nasal splint is a rigid or partially rigid device intended for use externally for immobilization of parts of the nose.

• Non-Rebreathing Valve (FDA Code: CBP / 868.5870)

A nonrebreathing valve is a one-way valve that directs breathing gas flow to the patient and vents exhaled gases into the atmosphere.

• Occlusive Wound Dressing (FDA Code: NAD / 878.4020)

An occlusive wound dressing is a nonresorbable, sterile or non-sterile device intended to cover a wound, to provide or support a moist wound environment, and to allow the exchange of gases such as oxygen and water vapor through the device. It consists of a piece of synthetic polymeric material, such as polyurethane, with or without an adhesive backing. This classification does not include an occlusive 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.

• Otological Strips

• Packings

• Pharyngeal Tubes

• Salivary Bypass Tubes

• Sinus Cannula (FDA Code: KAM / 878.4800)

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.

• Speaking Valves

• Stent Applicators

• Stent Dilators

• Suprastomal Stents

• Surgical Cutter (FDA Code: FZT / 878.4800)

• Thyroplasty Implant Systems

• Tracheal Tube Cleaning Brushes (FDA Code: EPE / 868.5795)

A tracheal tube cleaning brush is a device consisting of a brush with plastic bristles intended to clean tracheal cannula devices after their removal from patients.

• Tracheal Tube with/without Connector (FDA Code: BTR / 868.5730)

A tracheal tube is a device inserted into a patient's trachea via the nose or mouth and used to maintain an open airway.

• Tracheostomy Tube and Cuff (FDA Code: JOH / 868.5800)

A tracheostomy tube and tube cuff is a device intended to be placed into a surgical opening of the trachea to facilitate ventilation to the lungs. The cuff may be a separate or integral part of the tracheostomy tube and is, when inflated, intended to establish a seal between the tracheal wall and the tracheostomy tube. The cuff is used to prevent the patient's aspiration of substances, such as blood or vomit, or to provide a means for positive-pressure ventilation of the patient. This device is made of either stainless steel or plastic.

• Tracheostomy Tube with/without Connector (FDA Code: BTO / 868.5800)

• Tracheostomy Tubes

• Tympanostomy Tube (FDA Code: ETD / 874.3880)

A tympanostomy tube is a device that is intended to be implanted for ventilation or drainage of the middle ear. The device is inserted through the tympanic membrane to permit a free exchange of air between the outer ear and middle ear. A type of tympanostomy tube known as the malleous clip tube attaches to the malleous to provide middle ear ventilation. The device is made of materials such as polytetrafluoroethylene, polyethylene, silicon elastomer, or porous polyethylene.