The Torrent Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What The Torrent Corp. makes
The Torrent Corp. manufactures single-use surgical items, including the Stockinette for wound coverage and compression, sterile gauze fluff for wound care, and tongue depressors for medical examinations.
These products are regulated under FDA Class I and Class II designations, with some devices requiring 510(k) clearance. The company’s devices are listed in the FDA’s 510(k) registry and are based in the United States.
Catalogue
Stockinette, Surgical Ref K770621
Regimes: 510(k) Registry: 510(k)Gauze Fluff Ref K780394
Regimes: 510(k) Registry: 510(k)Tongue Depressor Ref K842461
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Torrent Corp. have in the registry?
The registry currently lists 3 devices for The Torrent Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Torrent Corp.'s devices?
Among its 3 most recently registered devices, The Torrent Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do The Torrent Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for The Torrent Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Torrent Corp. in the registry?
The most recently registered devices listed for The Torrent Corp. include STOCKINETTE, SURGICAL, GAUZE FLUFF and TONGUE DEPRESSOR.