Baylab Usa
Also registered as Baylab USA, LLC
Country not established FDA establishment FEI 3017517827
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
BAYLAB 3-Ply Surgical Mask (BEACON I) Ref K212302
510(k) 510(k)
Company details
- FDA FEI number
- 3017517827
- Address
- 2230 LBJ FREEWAY, Dallas, TX, 75234
Frequently asked questions
How many devices does BAYLAB USA have in the registry?
The registry currently lists 8 devices for BAYLAB USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list BAYLAB USA's devices?
Among its 8 most recently registered devices, BAYLAB USA has devices listed in FDA 510(k) (1 device) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do BAYLAB USA's devices fall under?
Among its 8 most recently registered devices, the classes recorded for BAYLAB USA's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BAYLAB USA in the registry?
The most recently registered devices listed for BAYLAB USA include BAYLAB USA 31CG6004-TRQ-XSR, BAYLAB USA 31CG6004-TRQ-SMR, BAYLAB USA 31CG6004-TRQ-MDR and BAYLAB USA 31CG6004-TRQ-LGR.