RecoveryRx 088
RecoveryRx 088 (214-4) is a Class II device made by Bioelectronics Corporation, listed in FDA GUDID since 3 Mar 2021 (UDI-DI 00851329005128), 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 | Number00851329005128 | Date3 Mar 2021 | StatusListed |
Official records
- AccessGUDID record 00851329005128
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- RecoveryRx
- Generic name
- Hand-held deep-tissue electromagnetic stimulator
- Model / Ref / Catalog
- 088, 214-4
- Primary DI / UDI-DI
- 00851329005128
- FDA product code
- PQY, ILX
- GMDN term
- Hand-held deep-tissue electromagnetic stimulator
- Device class
- Class II
- Regulation number
- 890.5290
- GUDID distribution status
- In Commercial Distribution
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