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DentaIBT

ASIGA PTY LTD · Model 03746 · UDI-DI 09359215000055

QJJ Prescription
0
510(k) clearances
1
Adverse events
1
Recalls
38
Facilities

Recalls

DateFirmReason
2026-06-08Klowen BracesA product error defect may cause incorrect bracket placement.

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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.