Dr. Howard Martin, P.A.
Country not established
- Devices
- 3
What Dr. Howard Martin, P.A. makes
Dr. Howard Martin, P.A. manufactures endodontic materials, including gutta percha-based sealers infused with tetracycline or doxycycline for root canal therapy, as well as medicated canal sealers and antibacterial gutta percha formulations.
Their products are regulated under FDA’s 510(k) pathway, with devices classified as Class I or Class II, and are listed in the FDA’s 510(k) database. The company operates in the United States.
Catalogue
- 510(k) 510(k)
Mcs-Medicated Canal Sealer Ref K973636
510(k) 510(k)Antibacterial Gutta Percha Ref K971641
510(k) 510(k)
Frequently asked questions
How many devices does Dr. Howard Martin, P.A. have in the registry?
The registry currently lists 3 devices for Dr. Howard Martin, P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Howard Martin, P.A.'s devices?
Among its 3 most recently registered devices, Dr. Howard Martin, P.A. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dr. Howard Martin, P.A.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dr. Howard Martin, P.A.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Howard Martin, P.A. in the registry?
The most recently registered devices listed for Dr. Howard Martin, P.A. include TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE), MCS-MEDICATED CANAL SEALER and ANTIBACTERIAL GUTTA PERCHA.