Penn-Med Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Penn-Med Technology, Inc. makes
Penn-Med Technology, Inc. makes dental devices including a bur, dental gutta percha-file-pulp canal, and a curing light.
These devices are classified as Class I and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Bur, Dental Gutta Percha-File-Pulp Canal Ref K842720
Regimes: 510(k) Registry: 510(k)Dental Handpiece Ref K840690
Regimes: 510(k) Registry: 510(k)Curing Light Ref K843049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Penn-Med Technology, Inc. have in the registry?
The registry currently lists 3 devices for Penn-Med Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Penn-Med Technology, Inc.'s devices?
Among its 3 most recently registered devices, Penn-Med Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Penn-Med Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Penn-Med Technology, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Penn-Med Technology, Inc. in the registry?
The most recently registered devices listed for Penn-Med Technology, Inc. include BUR, DENTAL GUTTA PERCHA-FILE-PULP CANAL, DENTAL HANDPIECE and CURING LIGHT.