Tybr Health, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3027383505
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
TYBR Collagen Gel Ref K250109
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3027383505
- Address
- 2450 Holcombe Blvd Ste X, Houston, TX, 77021
Frequently asked questions
How many devices does TYBR HEALTH, INC. have in the registry?
The registry currently lists 2 devices for TYBR HEALTH, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list TYBR HEALTH, INC.'s devices?
Among its 2 most recently registered devices, TYBR HEALTH, INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do TYBR HEALTH, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for TYBR HEALTH, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from TYBR HEALTH, INC. in the registry?
The most recently registered devices listed for TYBR HEALTH, INC. include B3 GEL System B3TNP04061 and TYBR Collagen Gel.