FDA Device Intelligence
HomeSAGEMAX BIOCERAMICS, INC › Brylic™ / W-98-25-BR-D200-SD

Brylic™ / W-98-25-BR-D200-SD

SAGEMAX BIOCERAMICS, INC · Model W-82151 · UDI-DI 00842271129017

EBG
10
510(k) clearances
122
Adverse events (1 deaths)
4
Recalls
181
Facilities

Recalls

DateFirmReason
2020-10-09Talladium IncHeat-cured polymethylmethacrylate (PMMA) milling blank product used to make long-term temporary crowns and bridge restorations has incorrect label. label states Part no. 5336-B1 (
2009-10-22Jeneric/PentronPentron Clinical Technologies LLC received two (2) complaints alleging that the TempSpan Dual-Cure Temporary Crown and Bridge Material was not setting. Investigation of product in
2004-06-07Lang Dental Mfg Co, Inc.The dental acrylic resin powders are contaminated with small black particles believed to be polyethylene.
2004-06-07Lang Dental Mfg Co, Inc.The dental acrylic resin powders are contaminated with small black particles believed to be polyethylene.

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.