Home › HAAG-STREIT USA, INC. › Reliance
Reliance
HAAG-STREIT USA, INC. · Model FXM920 Chair · UDI-DI 00850020301034
10
510(k) clearances
11
Adverse events
1
Recalls
33
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-05-31 | UFSK - International OSYS Gmbh | Service life of the electrical seat part drive of the treatment chair may be shortened unexpectedly after several years of use due to a potential wear-related reduction in the self |
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.