Medtek Devices, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Medtek Devices, Inc. makes
Medtek Devices, Inc. manufactures the LAPEVAC, a filtration device designed for the peritoneum, and the PLUMEPEN, an integrated smoke evacuation pencil for surgical applications.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Lapevac, Filtration Device For The Periotoneum Ref K052797
510(k) 510(k)Plumepen Integrated Smoke Evacuation Pencil Ref K103375
510(k) 510(k)
Frequently asked questions
How many devices does Medtek Devices, Inc. have in the registry?
The registry currently lists 2 devices for Medtek Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtek Devices, Inc.'s devices?
Among its 2 most recently registered devices, Medtek Devices, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medtek Devices, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medtek Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtek Devices, Inc. in the registry?
The most recently registered devices listed for Medtek Devices, Inc. include LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM and PLUMEPEN INTEGRATED SMOKE EVACUATION PENCIL.