Ortho Spectrum, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ortho Spectrum, Inc. makes
Ortho Spectrum, Inc. manufactures orthopaedic staples and a Titan separating spring.
The company's products are listed in the FDA 510(k) registry and include Class I and Class II devices. Ortho Spectrum, Inc. is based in the US.
Catalogue
Orthopaedic Staples Ref K890962
Regimes: 510(k) Registry: 510(k)Titan Separating Spring Ref K930202
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ortho Spectrum, Inc. have in the registry?
The registry currently lists 2 devices for Ortho Spectrum, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ortho Spectrum, Inc.'s devices?
Among its 2 most recently registered devices, Ortho Spectrum, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ortho Spectrum, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ortho Spectrum, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ortho Spectrum, Inc. in the registry?
The most recently registered devices listed for Ortho Spectrum, Inc. include ORTHOPAEDIC STAPLES and TITAN SEPARATING SPRING.