Ultradent Products, Inc.

Ultradent Products, Inc. holds 104 FDA 510(k) medical device clearances, first cleared 1992, most recent 2026, with 20 FDA device recalls on record.

Clearances by Ultradent Products, Inc. — page 2

101–104 of 104

K921409 — ENAMEL AND PORCELAIN ETCH PRODUCT LINECode EBF·1992-09-09
K921598 — ULTRADENT PRODUCT PIT & FISSURE SEALANT PROD LINECode EBF·1992-09-09
K921602 — ULTRADENT PRODUCT TOOTH SURFACE DRYING AGENTCode EBF·1992-09-09
K921601 — ULTRADENT PROD RETRACT CORD/ACCESSORY PRODUCT LINECode JES·1992-06-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.