Bruce Medical Supply
United Statesfrom the FDA registration address FDA establishment FEI 1220479
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Bruce Medical Supply makes
Bruce Medical Supply manufactures the Lectro-Larynx, a device designed for individuals with vocal cord dysfunction or laryngectomy patients to produce speech by converting electrical signals into audible sound.
The Lectro-Larynx is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Lectro-Larynx Ref K923648
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1220479
- Address
- 411 Waverley Oaks Rd Ste 154, Waltham, MA, 02452
Frequently asked questions
How many devices does BRUCE MEDICAL SUPPLY have in the registry?
The registry currently lists 1 device for BRUCE MEDICAL SUPPLY. Devices recorded under merged duplicate company entries are counted once.
Which registries list BRUCE MEDICAL SUPPLY's devices?
Among its 1 most recently registered device, BRUCE MEDICAL SUPPLY has devices listed in FDA 510(k) (1 device).
What risk classes do BRUCE MEDICAL SUPPLY's devices fall under?
Among its 1 most recently registered device, the classes recorded for BRUCE MEDICAL SUPPLY's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from BRUCE MEDICAL SUPPLY in the registry?
The most recently registered devices listed for BRUCE MEDICAL SUPPLY include LECTRO-LARYNX.