Home › INNOVATION INSTITUTE, LLC › LiveBand BFR
LiveBand BFR
INNOVATION INSTITUTE, LLC · Model 3185-90007 · UDI-DI 00850055775077
10
510(k) clearances
1,994
Adverse events (1 deaths)
111
Recalls
108
Facilities
Description
The LiveBand Blood Flow Restriction System is a portable and user-friendly Blood Flow Restriction device. BFR training is clinically proven to increase muscle strength and aid in physical and rehabilitation therapy, while reducing the weight load on joints. LiveBand BFR uses a proprietary system to actively manage and maintain the desired limb occlusion pressure, customized for each patient.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
| 2026-08-24 | ASP Global, LLC. | Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.