Robert Reid, Inc.
United StatesFDA applicant, unverified FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Robert Reid, Inc. makes
Robert Reid, Inc. manufactures orthopedic fixation devices, including the KAPSS Spinal System for spinal stabilization and the MAGNUM Nail for internal fixation in long bone fractures.
These products are classified as Class II devices under FDA regulations and are authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Kapss Spinal System Ref K093833
Regimes: 510(k) Registry: 510(k)Magnum Nail Ref K093089
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Robert Reid Inc. Tokyo · JP FEI 3008198024
Frequently asked questions
How many devices does Robert Reid, Inc. have in the registry?
The registry currently lists 2 devices for Robert Reid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Robert Reid, Inc.'s devices?
Among its 2 most recently registered devices, Robert Reid, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Robert Reid, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Robert Reid, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Robert Reid, Inc. in the registry?
The most recently registered devices listed for Robert Reid, Inc. include KAPSS SPINAL SYSTEM and MAGNUM NAIL.
Which FDA establishments are linked to Robert Reid, Inc.?
1 FDA establishment is linked to Robert Reid, Inc. in the registry; they are listed on the company page.