Solcoor, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Solcoor, Inc. makes
Solcoor, Inc. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the AGAR 9K, AGAR 7K, and UNI-TENS series, designed for pain management. Their neuromuscular stimulators, such as the AGAR 4000 and AGAR 3K, are intended for muscle stimulation and rehabilitation. The company also produces peak flowmeters for spirometry, used in respiratory assessments.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Solcoor, Inc. is based in the United States.
Catalogue
Agar 9K Tens Ref K861894
Regimes: 510(k) Registry: 510(k)Peak Flowmeters For Spirometry Ref K851265
Regimes: 510(k) Registry: 510(k)Agar 4000 Neuromuscular Stimulator Ref K882387
Regimes: 510(k) Registry: 510(k)Agar 7K Tens Instrument Ref K862454
Regimes: 510(k) Registry: 510(k)Uni-Tens Xl Tens Ref K861896
Regimes: 510(k) Registry: 510(k)Agar 3K Neuromuscular Stimulator Ref K882386
Regimes: 510(k) Registry: 510(k)Uni-Tens Ref K861895
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Solcoor, Inc. have in the registry?
The registry currently lists 7 devices for Solcoor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Solcoor, Inc.'s devices?
Among its 7 most recently registered devices, Solcoor, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Solcoor, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Solcoor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Solcoor, Inc. in the registry?
The most recently registered devices listed for Solcoor, Inc. include AGAR 9K TENS, PEAK FLOWMETERS FOR SPIROMETRY, AGAR 4000 NEUROMUSCULAR STIMULATOR and AGAR 7K TENS INSTRUMENT.