Home › Sprintray, Inc. › IDB 2
IDB 2
Sprintray, Inc. · Model SRI-0202012 · UDI-DI 00850039704055
0
510(k) clearances
1
Adverse events
1
Recalls
38
Facilities
Description
Indicated for the fabrication, by additive manufacturing, of Indirect Bonding Tray
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-08 | Klowen Braces | A product error defect may cause incorrect bracket placement. |
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.