Ortho Kinetics Corp.
Country not established FDA establishment FEI 1000160800
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
What Ortho Kinetics Corp. makes
Ortho Kinetics Corp. makes orthodontic devices including reverse pull facemasks, releasable force modules, facebows, power coins glow-in-the-dark ligatures, new gear releasable headgear, Affirm Smart releasable force module and compliance science system, and Nitom locking facebows.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Class Iii Reverse Pull Facemask Ref K980436
510(k) 510(k)Releasable Force Module Ref K980151
510(k) 510(k)Facebow Ref K980195
510(k) 510(k)Power Coins Glow In The Dark Ligatures Ref K980864
510(k) 510(k)New Gear Releasable Headgear Ref K940410
510(k) 510(k)- 510(k) 510(k)
Nitom Locking Facebow Ref K980245
510(k) 510(k)
Company details
- FDA FEI number
- 1000160800
- Address
- 2588 Progress St Ste 13, VISTA, CA, 92081
Frequently asked questions
How many devices does ORTHO KINETICS CORP. have in the registry?
The registry currently lists 7 devices for ORTHO KINETICS CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORTHO KINETICS CORP.'s devices?
Among its 7 most recently registered devices, ORTHO KINETICS CORP. has devices listed in FDA 510(k) (7 devices).
What risk classes do ORTHO KINETICS CORP.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for ORTHO KINETICS CORP.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from ORTHO KINETICS CORP. in the registry?
The most recently registered devices listed for ORTHO KINETICS CORP. include CLASS III REVERSE PULL FACEMASK, RELEASABLE FORCE MODULE, FACEBOW and POWER COINS GLOW IN THE DARK LIGATURES.