Allmed Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
What Allmed Systems, Inc. makes
Allmed Systems, Inc. makes Revolix and Revolix JR laser systems, including models such as Revolix 120, Revolix JR 30, Revolix JR 50, Revolix JR 160, Revolix FR 200, Revolix Duo Laser System, and Sphinx Laser Systems, as well as the Sphinx JR and FlexGuard devices.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Revolix 120 Ref K070476
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Revolix Laser Systems Ref K033423
Regimes: 510(k) Registry: 510(k)Revolix Duo Laser System Ref K070466
Regimes: 510(k) Registry: 510(k)Sphinx Jr Ref K132975
Regimes: 510(k) Registry: 510(k)Revolix And Revolix Jr Ref K051167
Regimes: 510(k) Registry: 510(k)Flexguard Ref K070924
Regimes: 510(k) Registry: 510(k)Sphinx Laser Systems Ref K033437
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Allmed Systems, Inc. have in the registry?
The registry currently lists 8 devices for Allmed Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allmed Systems, Inc.'s devices?
Among its 8 most recently registered devices, Allmed Systems, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Allmed Systems, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Allmed Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Allmed Systems, Inc. in the registry?
The most recently registered devices listed for Allmed Systems, Inc. include REVOLIX 120, REVOLIX JR 30, REVOLIX JR 50, REVOLIX JR 160, REVOLIX FR 200, REVOLIX LASER SYSTEMS and REVOLIX DUO LASER SYSTEM.