Gvs Tm, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2013342
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 11 ongoing
Catalogue
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 2013342
- Address
- 1630 W Industrial Park St, Covina, CA, 91722
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 1
- 2026 0
2025
- 3 Nov 2025 Z-1157-2026 Class II Ongoing Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.
Frequently asked questions
How many devices does GVS TM, INC. have in the registry?
The registry currently lists 2 devices for GVS TM, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list GVS TM, INC.'s devices?
Among its 2 most recently registered devices, GVS TM, INC. has devices listed in FDA GUDID (2 devices).
What risk classes do GVS TM, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for GVS TM, INC.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for GVS TM, INC.?
FDA recall records list 1 recall initiated by GVS TM, INC., the most recent initiated on 3 Nov 2025. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from GVS TM, INC. in the registry?
The most recently registered devices listed for GVS TM, INC. include GVS SQ40s and GVS LPS2KLE.