Pathway MR-20
by Prometheus Group of New Hampshire Limited, the
Pathway MR-20 (9710) is a Class II device made by Prometheus Group of New Hampshire Limited, the, listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00852423006059), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00852423006059 | Date26 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00852423006059
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pathway
- Generic name
- Perineometer
- Model / Ref / Catalog
- MR-20, 9710
- Primary DI / UDI-DI
- 00852423006059
- FDA product code
- HIR
- GMDN term
- Perineometer
- Device class
- Class II
- Regulation number
- 884.1425
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code HIR (Perineometer).
- SRS Vaginal EMG/Stimulation Perineometer Sensor SRS Anal EMG/Stimulation Perineometer Sensor by SRS Medical Systems, Inc.
- Incontrol Perineometer by THOUGHT TECHNOLOGY LTD.
- Intimate Rose Kegel Exercise System by Plus EV Holdings Dba Intimate Rose
- GYNEFLEX by Naissance Holdings, LC
- INNOVA VAGINAL EMG SENSING ELECTRODE by Empi
- PERITRON by Cardio Design Pty., Ltd.
- Flyte Mechanotherapy System (aka Flyte System) (MTI-1.0) by Pelvital USA, Inc.
- IEVA REHABILITATIVE POSITIONAL DEVICE by Remendium Labs, LLC
- PERINEOMETER by Hollister, Inc.
- PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE) by BIOSEARCH MEDICAL PRODUCTS, INC.
Other devices from Prometheus Group of New Hampshire Limited, the
See all devices from Prometheus Group of New Hampshire Limited, the →