Home › CANDID CARE CO. › Candid Aligner
Candid Aligner
CANDID CARE CO. · Model FA-0001 · UDI-DI 08500042230004
NXC
Prescription
1
510(k) clearances
18,497
Adverse events (1 deaths)
2
Recalls
99
Facilities
Description
Candid Aligner System FA-0001
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-11-22 | 3M Company - Health Care Business | Attachments may not mate with the tooth as intended in the digital treatment design. |
| 2024-11-04 | Straight Smile, LLC | Virtual-only clinical workflow utilized for dental aligners and impression to approve patients for aligner devices may not be suitable for patients who have certain contraindicatio |
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.