United States Dental Laser, Inc.

United States Dental Laser, Inc. holds 1 FDA 510(k) medical device clearance, cleared in 1995.

Top product codes for United States Dental Laser, Inc.

GEX — General, Plastic Surgery1 device

Recent clearances by United States Dental Laser, Inc.

K943638 — USDL MODEL SELECT 1000 FREQUENCY DOUBLED ND:YAG LASER SYSTEMCode GEX·1995-03-06

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