Medical Monofilament Manufacturing
United Statesfrom the FDA registration address FDA establishment FEI 3002957596
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Medical Monofilament Sensory Screening Toool Ref K143068
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3002957596
- Address
- 121 Camelot Dr Ste 2, Plymouth, MA, 02360
Frequently asked questions
How many devices does MEDICAL MONOFILAMENT MANUFACTURING have in the registry?
The registry currently lists 1 device for MEDICAL MONOFILAMENT MANUFACTURING. Devices recorded under merged duplicate company entries are counted once.
Which registries list MEDICAL MONOFILAMENT MANUFACTURING's devices?
Among its 1 most recently registered device, MEDICAL MONOFILAMENT MANUFACTURING has devices listed in FDA 510(k) (1 device).
What risk classes do MEDICAL MONOFILAMENT MANUFACTURING's devices fall under?
Among its 1 most recently registered device, the classes recorded for MEDICAL MONOFILAMENT MANUFACTURING's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from MEDICAL MONOFILAMENT MANUFACTURING in the registry?
The most recently registered devices listed for MEDICAL MONOFILAMENT MANUFACTURING include Medical Monofilament Sensory Screening Toool.