FDA Device Intelligence
Home3M COMPANY › 3M™ Unitek™

3M™ Unitek™

3M COMPANY · Model 900215 · UDI-DI 30605861027596

ELZ Prescription
9
510(k) clearances
22
Adverse events
4
Recalls
134
Facilities

Description

3M™ Unitek™ Stainless Steel Second Primary Molar Crown, Upper Left, Size 5 (5/pack), 900215

Recalls

DateFirmReason
2013-08-053M Company/3m Espe Dental Products3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary UL4) because these products have been manufactured with the incorrect marginal contour edge.
2013-06-053M Company - Health Care Business3M is recalling specific lots of 3M ESPE Unitek Primary Stainless Steel Crowns - Series UR4 contain LL3 crowns which are incorrectly labeled as UR4 crowns.
2010-10-063M Company / Medical DivisionUnitek Stainless Steel Permanent Crowns with product Codes 902150, 900213, and 900223, is mislabeled. The crown contained within the package is incorrectly labeled; series UL3 crow
2007-10-173M Company / Medical DivisionMislabeled: Unitek Stainless Steel Permanent Molar Crowns were placed in packaging which incorrectly identified the product as Unitek Stainless Steel Primary Molar Crowns.

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.