Rebound Rebound Health
by BioMedical Life Systems Inc.
Rebound Health (KBTR) is a medical device (FDA Class II; FDA product code NUH, Stimulator, Nerve, Transcutaneous, Over-The-Counter) made by BioMedical Life Systems Inc., cleared under FDA 510(k) K102051 on 29 Jul 2011 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00857771003019), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00857771003019 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK102051 | Date29 Jul 2011 | StatusActive |
Official records
- AccessGUDID record 00857771003019
- FDA 510(k) database K102051
Across registries
- FDA 510(k) K102051 decided 29 Jul 2011 Active
- FDA GUDID UDI-DI 00857771003019 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K102051
- Listed FDA GUDID 00857771003019
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Rebound
- Generic name
- Analgesic transcutaneous electrical nerve stimulation system
- Model / Ref / Catalog
- Rebound Health, KBTR
- Primary DI / UDI-DI
- 00857771003019
- 510(k) Number
- FDA product code
- NUH
- GMDN term
- Analgesic transcutaneous electrical nerve stimulation system
- Device class
- Class II
- Regulation number
- 882.5890
- GUDID distribution status
- In Commercial Distribution
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