Quick-Med Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Quick-Med Technologies, Inc. makes
Quick-Med Technologies, Inc. makes skin fold management textiles and antimicrobial barrier gauze dressings, including the Stay Fresh Skin Fold Management Textile and the QMT Nimbus Antimicrobial Barrier Gauze Dressing.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Stay Fresh Skin Fold Management Textile Ref K121898
Regimes: 510(k) Registry: 510(k)Qmt Nimbus Antimicrobial Barrier Gauze Dressing Ref DEN070002
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Quick-Med Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Quick-Med Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quick-Med Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Quick-Med Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Quick-Med Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Quick-Med Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quick-Med Technologies, Inc. in the registry?
The most recently registered devices listed for Quick-Med Technologies, Inc. include STAY FRESH SKIN FOLD MANAGEMENT TEXTILE and QMT NIMBUS ANTIMICROBIAL BARRIER GAUZE DRESSING.