Biotex, Inc.
United StatesFDA applicant, unverified FDA FEI 3005726841
Biotex, Inc. is a medical device manufacturer, with 41 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 15 Nov 2026.
- Devices
- 41
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 31
- FDA 510(k) 10
- Device classes
- FDA Class II 27
- FDA Class I 14
- Identifiers
- FDA FEI 3005726841
- DUNS 969792050
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 41 devicesCompany details
- FDA FEI number
- 3005726841
- DUNS number
- 969792050
- Address
- 114 Holmes Rd, HOUSTON, TX, 77045
- xx@xx.xx
- Phone
- 7137410111
Frequently asked questions
How many devices does BIOTEX, INC. have in the registry?
The registry currently lists 41 devices for BIOTEX, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list BIOTEX, INC.'s devices?
Among its 41 most recently registered devices, BIOTEX, INC. has devices listed in FDA 510(k) (10 devices) and FDA GUDID (31 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do BIOTEX, INC.'s devices fall under?
Among its 41 most recently registered devices, the classes recorded for BIOTEX, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from BIOTEX, INC. in the registry?
The most recently registered devices listed for BIOTEX, INC. include Bayou™ troCarWash System Disposable Kit TCW-5-100, OcciGuide 048-1000, Bayou™ troCarWash System Disposable Kit 038-1000 and Phasor Drill 008-1042.