Implant Corp. of America
United StatesFDA applicant, unverified
- Devices
- 3
What Implant Corp. of America makes
Implant Corp. of America manufactures surgical instruments designed for orthopedic and dental procedures, including paralleling guides for precise implant alignment, bone drills and taps for osteotomy preparation, and ADA shank extensions for compatibility with standard handpieces.
Their portfolio includes devices classified under FDA regulations as Class I and Class II, with submissions documented through the 510(k) clearance pathway. The company’s products are listed in the FDA’s regulatory database, and the manufacturer is based in the United States.
Catalogue
Paralleling Guides Ref K914715
Regimes: 510(k) Registry: 510(k)Bone Drills Or Taps Ref K914714
Regimes: 510(k) Registry: 510(k)Ada Shank Extension Ref K914724
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Implant Corp. of America have in the registry?
The registry currently lists 3 devices for Implant Corp. of America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Implant Corp. of America's devices?
Among its 3 most recently registered devices, Implant Corp. of America has devices listed in FDA 510(k) (3 devices).
What risk classes do Implant Corp. of America's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Implant Corp. of America's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Implant Corp. of America in the registry?
The most recently registered devices listed for Implant Corp. of America include PARALLELING GUIDES, BONE DRILLS OR TAPS and ADA SHANK EXTENSION.