Protech Leaded Eyewear, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000488948
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 1000488948
- Address
- 7960 Central Industrial Drive, West Palm Beach, FL, 33404
Frequently asked questions
How many devices does PROTECH LEADED EYEWEAR, INC. have in the registry?
The registry currently lists 4 devices for PROTECH LEADED EYEWEAR, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PROTECH LEADED EYEWEAR, INC.'s devices?
Among its 4 most recently registered devices, PROTECH LEADED EYEWEAR, INC. has devices listed in FDA GUDID (4 devices).
What risk classes do PROTECH LEADED EYEWEAR, INC.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for PROTECH LEADED EYEWEAR, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from PROTECH LEADED EYEWEAR, INC. in the registry?
The most recently registered devices listed for PROTECH LEADED EYEWEAR, INC. include Apollo APO-FB-ST-SM, Apollo APO-FB-ST-MD, Apollo APO-FB-ST-LG and Apollo APO-FB-ST-XL.