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Reliance

HAAG-STREIT USA, INC. · Model 558 Stool · UDI-DI 00850020301249

BRX
1
510(k) clearances
2
Adverse events
1
Recalls
2
Facilities

Recalls

DateFirmReason
2019-07-10Gk Photonics IncThe User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.