Progressive Surgical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Progressive Surgical Products, Inc. makes
Progressive Surgical Products, Inc. manufactures PROXIDERM surgical drapes and gowns, including models TN 460, TN 90 460, BK 460, D-460, D 90 460, D 180, 460, and PS 460, as well as a tentative PROXIDERM variant. These products are designed for use in surgical procedures to maintain sterile fields and protect patients and staff.
The company’s products fall under FDA Class I medical devices and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Proxiderm, Models Tn 460, Tn 90 460, Bk 460 Ref K982439
Regimes: 510(k) Registry: 510(k)Proxiderm (D-460, D 90 460, D 180, 460, Ps 460) Ref K970439
Regimes: 510(k) Registry: 510(k)Proxiderm (Tentative) Ref K942425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Progressive Surgical Products, Inc. have in the registry?
The registry currently lists 3 devices for Progressive Surgical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Progressive Surgical Products, Inc.'s devices?
Among its 3 most recently registered devices, Progressive Surgical Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Progressive Surgical Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Progressive Surgical Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Progressive Surgical Products, Inc. in the registry?
The most recently registered devices listed for Progressive Surgical Products, Inc. include PROXIDERM, MODELS TN 460, TN 90 460, BK 460, PROXIDERM (D-460, D 90 460, D 180, 460, PS 460) and PROXIDERM (TENTATIVE).