Newmark, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Newmark, Inc. makes
Newmark, Inc. manufactures transdermal drug delivery systems, specifically the Painmaster MCT Patch, designed for controlled medication administration through the skin.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Painmaster Mct Patch Ref K090042
Regimes: 510(k) Registry: 510(k)Painmaster Mct Patch Ref K130114
Regimes: 510(k) Registry: 510(k)Painmaster MCT Patch Ref K151995
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Newmark, Inc. have in the registry?
The registry currently lists 3 devices for Newmark, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Newmark, Inc.'s devices?
Among its 3 most recently registered devices, Newmark, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Newmark, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Newmark, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Newmark, Inc. in the registry?
The most recently registered devices listed for Newmark, Inc. include PAINMASTER MCT PATCH.