Vision Quest Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Vision Quest Industries, Inc. makes
Vision Quest Industries, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the T.E.A.R. TECH3 (Model #44TT03 and base model), FAST START TENS (Model FS 3001), and surgical stimulation systems like the SURGI STIM. The company also produces reusable medical electrodes, such as the TARGET STERILE ELECTRODE, and a hand rehabilitation system called the BioniCare Hand System.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
T.E.A.R. TECH3 Model #44TT03 Ref K030507
Regimes: 510(k) Registry: 510(k)T.E.A.R. TECH3 Ref K090532
Regimes: 510(k) Registry: 510(k)Surgi Stim Ref K982388
Regimes: 510(k) Registry: 510(k)Fast Start Tens, Model Fs 3001 Ref K041092
Regimes: 510(k) Registry: 510(k)Target Sterile Electrode Ref K072799
Regimes: 510(k) Registry: 510(k)BioniCare Hand System Ref K142236
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vision Quest Industries, Inc. have in the registry?
The registry currently lists 6 devices for Vision Quest Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vision Quest Industries, Inc.'s devices?
Among its 6 most recently registered devices, Vision Quest Industries, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Vision Quest Industries, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Vision Quest Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vision Quest Industries, Inc. in the registry?
The most recently registered devices listed for Vision Quest Industries, Inc. include T.E.A.R. TECH3 MODEL #44TT03, T.E.A.R. TECH3, SURGI STIM and FAST START TENS, MODEL FS 3001.