Neuromuscular Technologies, Inc.
Country not established
- Devices
- 1
What Neuromuscular Technologies, Inc. makes
Neuromuscular Technologies, Inc. manufactures the Dolotens Dental™ 1, a dental device designed for neuromuscular dentistry applications, including temporomandibular joint (TMJ) treatment and occlusal analysis.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Dolotens Dental™ 1 authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Dolotens Dental Tm 1 Ref K043373
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuromuscular Technologies, Inc. have in the registry?
The registry currently lists 1 device for Neuromuscular Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuromuscular Technologies, Inc.'s devices?
Among its 1 most recently registered device, Neuromuscular Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neuromuscular Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuromuscular Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuromuscular Technologies, Inc. in the registry?
The most recently registered devices listed for Neuromuscular Technologies, Inc. include DOLOTENS DENTAL TM 1.