Fla Orthopedics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Fla Orthopedics, Inc. makes
Fla Orthopedics, Inc. manufactures patient restraint devices designed for use in clinical and healthcare settings to secure patients during medical procedures or transport.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Restraint Ref K970272
Regimes: 510(k) Registry: 510(k)Patient Restraints Ref K970274
Regimes: 510(k) Registry: 510(k)Patient Restraints Ref K970273
Regimes: 510(k) Registry: 510(k)Patient Restraints Ref K970275
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fla Orthopedics, Inc. have in the registry?
The registry currently lists 4 devices for Fla Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fla Orthopedics, Inc.'s devices?
Among its 4 most recently registered devices, Fla Orthopedics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Fla Orthopedics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Fla Orthopedics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fla Orthopedics, Inc. in the registry?
The most recently registered devices listed for Fla Orthopedics, Inc. include PATIENT RESTRAINT and PATIENT RESTRAINTS.