The Prometheus Group
Country not established FDA establishment FEI 1000513601
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 11 devicesCompany details
- FDA FEI number
- 1000513601
- Address
- 1 WASHINGTON ST., SUITE 3171, DOVER, NH, 03820
Frequently asked questions
How many devices does THE PROMETHEUS GROUP have in the registry?
The registry currently lists 11 devices for THE PROMETHEUS GROUP. Devices recorded under merged duplicate company entries are counted once.
Which registries list THE PROMETHEUS GROUP's devices?
Among its 11 most recently registered devices, THE PROMETHEUS GROUP has devices listed in FDA 510(k) (11 devices).
What risk classes do THE PROMETHEUS GROUP's devices fall under?
Among its 11 most recently registered devices, the classes recorded for THE PROMETHEUS GROUP's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from THE PROMETHEUS GROUP in the registry?
The most recently registered devices listed for THE PROMETHEUS GROUP include PATHWAY II ELECTROMYOGRAPH, PATHWAY STM-10 PELVIC FLOOR STIMULATOR, PATHWAY CTS 2000 PELVIC FLOOR TRAINING SYSTEM, MODEL PATHWAY CTS 2000 and PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25.