Talladium, Inc.
Talladium, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 2016, with 2 FDA device recalls on record.
Top product codes for Talladium, Inc.
FDA recalls by Talladium, Inc.
- Z-0512-2021 — Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional crowns and bridges. All blanks are solely used by a Trained Dental Technician or on the order of a dental professional.
- Z-2943-2020 — Talladium Luminesse Zirconia Discs, Zirconia HT Disc 98x20mm A1, Shaded Zirconia Blend 2.0 50# A1, Model No. 5147-A1;(UDI): D7915147A10 - Product Usage: are intended for CAD/CAM fabrication of all-ceramic (no metal) dental restorations. Luminesse ZR Blanks are partially sintered Yttria stabilized zirconia blanks for use as CAD/CAM milling blanks.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Talladium, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.