Avitar, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Avitar, Inc. makes
Avitar, Inc. manufactures absorbable sponges and sterile dressings designed for surgical and medical use, including the Hydrasorb Joyce Sponge and Hydrasorb sterile dressings. These products are formulated to absorb fluids and are used in wound care and surgical procedures to manage moisture and promote healing.
The company’s portfolio includes devices classified under Class I, Class II, and Unclassified (U) categories, with several products authorised via the FDA’s 510(k) pathway. These products are listed in the FDA’s regulatory database, and the company operates from the United States.
Catalogue
Hydrasorb Joyce Sponge Ref K925841
510(k) 510(k)Hydrasorb Sterile Dressing Ref K973260
510(k) 510(k)Hydrasorb(Tm) Ref K897156
510(k) 510(k)Hydrasorb(Tm) Ref K897102
510(k) 510(k)
Frequently asked questions
How many devices does Avitar, Inc. have in the registry?
The registry currently lists 4 devices for Avitar, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avitar, Inc.'s devices?
Among its 4 most recently registered devices, Avitar, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Avitar, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Avitar, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avitar, Inc. in the registry?
The most recently registered devices listed for Avitar, Inc. include HYDRASORB JOYCE SPONGE, HYDRASORB STERILE DRESSING and HYDRASORB(TM).