FDA Device Intelligence
Home › RELIANCE ORTHODONTIC PRODUCTS INC › BOND ALIGNER

BOND ALIGNER

RELIANCE ORTHODONTIC PRODUCTS INC · Model 1BA · UDI-DI 00840479200064

DYH
10
510(k) clearances
37
Adverse events (1 deaths)
1
Recalls
66
Facilities

Recalls

DateFirmReason
2007-10-31Ormco CorporationMislabeled: Product mislabeled with incorrect expiration date. Expiration date labeled as 2010/07 instead of 2009/07.

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 docs
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.