Verite
Country not established
- Devices
- 10
What Verite makes
Verite makes transcutaneous electrical nerve stimulation (TENS) devices, personal pain relievers, and related electrotherapy products, including models such as the 811 VERI/TENS & PO, VERIL/PPR PERSONAL PAIN RELIEVER #800, VERI-FIER, VERI/PMS MODEL 815, MODEL 810 VERI/TGS, VERI/DFS TM #817, MODEL 500 VERI/500, MODEL 860-1 VERI/PROBE, and MODEL 800-A VERI/PPR.
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
Model 1000 Ref K844727
Regimes: 510(k) Registry: 510(k)Model 811 Veri/Tens & Po Ref K840098
Regimes: 510(k) Registry: 510(k)Veril/Ppr Personal Pain Reliever #800 Ref K822929
Regimes: 510(k) Registry: 510(k)Veri-Fier Ref K811351
Regimes: 510(k) Registry: 510(k)Veri/Pms Model 815 Ref K810496
Regimes: 510(k) Registry: 510(k)Model 810 Veri/Tgs Ref K791187
Regimes: 510(k) Registry: 510(k)Veri/Dfs Tm #817 Ref K813515
Regimes: 510(k) Registry: 510(k)Model 500 Veri/500 Ref K813108
Regimes: 510(k) Registry: 510(k)Model 860-1 Veri/Probe Ref K820651
Regimes: 510(k) Registry: 510(k)Model 800-A Veri/Ppr Ref K840099
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Verite have in the registry?
The registry currently lists 10 devices for Verite. Devices recorded under merged duplicate company entries are counted once.
Which registries list Verite's devices?
Among its 10 most recently registered devices, Verite has devices listed in FDA 510(k) (10 devices).
What risk classes do Verite's devices fall under?
Among its 10 most recently registered devices, the classes recorded for Verite's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Verite in the registry?
The most recently registered devices listed for Verite include MODEL 1000, MODEL 811 VERI/TENS & PO, VERIL/PPR PERSONAL PAIN RELIEVER #800 and VERI-FIER.