Horizon Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Horizon Orthopedic Pin Protector Ref K883576
Regimes: 510(k) Registry: 510(k)Steri-Lub Lubrication Gel Ref K944969
Regimes: 510(k) Registry: 510(k)Dermasense Plus Dispersive Electrode Ref K980171
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Horizon Medical, Inc. have in the registry?
The registry currently lists 3 devices for Horizon Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Horizon Medical, Inc.'s devices?
Among its 3 most recently registered devices, Horizon Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Horizon Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Horizon Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Horizon Medical, Inc. in the registry?
The most recently registered devices listed for Horizon Medical, Inc. include HORIZON ORTHOPEDIC PIN PROTECTOR, STERI-LUB LUBRICATION GEL and DERMASENSE PLUS DISPERSIVE ELECTRODE.