Eforto
Uniweb · Model M1 Vigorimeter · UDI-DI 05430004547006
10
510(k) clearances
0
Adverse events
2
Recalls
17
Facilities
Description
Eforto M1 Vigorimeter
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-11-30 | Activbody, Inc. | Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and lis |
| 2021-11-30 | Activbody, Inc. | Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and lis |
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.