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KINVENT HELLAS · Model Bubble V2R01 · UDI-DI 03770011995448
10
510(k) clearances
0
Adverse events
2
Recalls
17
Facilities
Description
Bubble is a pneumatic sensor allowing you to work your strength with convenient inflatable tools.
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 |
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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.