Poly-Med, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3006121828
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3006121828
- Address
- 52 Technology Dr, Anderson, SC, 29625
Frequently asked questions
How many devices does POLY-MED, INC. have in the registry?
The registry currently lists 1 device for POLY-MED, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list POLY-MED, INC.'s devices?
Among its 1 most recently registered device, POLY-MED, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do POLY-MED, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for POLY-MED, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from POLY-MED, INC. in the registry?
The most recently registered devices listed for POLY-MED, INC. include EUROPLATE-CONDUCTIVE ADHESIVE ELECTROSURGICAL RETU.