Neotonus, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Neotonus, Inc. makes
Neotonus, Inc. manufactures neuromuscular stimulation devices, including the Model 1000 Muscle Stimulator System for muscle activation, the PNS Magnetic Stimulator System for peripheral nerve stimulation, and the Neocontrol Pelvic Floor Therapy System for pelvic floor rehabilitation. The company also produces the MS-101 Magnetic Muscle Stimulator System, designed for targeted muscle stimulation.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Neotonus Model 1000 Muscle Stimulator System Ref K973096
Regimes: 510(k) Registry: 510(k)Pns Magnetic Stimulator System Ref K002889
Regimes: 510(k) Registry: 510(k)Neocontrol Pelvic Floor Therapy System Ref K001903
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neotonus, Inc. have in the registry?
The registry currently lists 4 devices for Neotonus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neotonus, Inc.'s devices?
Among its 4 most recently registered devices, Neotonus, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Neotonus, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Neotonus, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neotonus, Inc. in the registry?
The most recently registered devices listed for Neotonus, Inc. include NEOTONUS MODEL 1000 MUSCLE STIMULATOR SYSTEM, PNS MAGNETIC STIMULATOR SYSTEM, NEOCONTROL PELVIC FLOOR THERAPY SYSTEM and NEOTONUS MS-101 MAGNETIC MUSCLE STIMULATOR SYSTEM.