Mediquest, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Mediquest, Inc. makes
Mediquest, Inc. manufactures skin staple removers and female external urinary collection pouches.
The company is based in the United States, and its portfolio consists of Class I medical devices that are listed in the FDA 510(k) registry.
Catalogue
Skin Staple Remover Ref K840089
Regimes: 510(k) Registry: 510(k)Female External Urinary Collection Pouch Ref K971499
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediquest, Inc. have in the registry?
The registry currently lists 2 devices for Mediquest, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediquest, Inc.'s devices?
Among its 2 most recently registered devices, Mediquest, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mediquest, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mediquest, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mediquest, Inc. in the registry?
The most recently registered devices listed for Mediquest, Inc. include SKIN STAPLE REMOVER and FEMALE EXTERNAL URINARY COLLECTION POUCH.