Lares Research, Inc.
Lares Research, Inc. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2014.
Top product codes for Lares Research, Inc.
Recent clearances by Lares Research, Inc.
- K141221 — LARES ULTRALITE PROSTYLE HIGH-SPEED DENTAL HANDPIECES, LARES EURO PROSTYLE HIGH-SPEED DENTAL HANDPIECES, LARES TURBO+ PR
- K031540 — APEX ELECTRIC HANDPIECE SYSTEM
- K011960 — LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS POCKETPRO OR POCKETPRO S4)
- K983524 — LARES RESEARCH SUNLASE 800P LASER SYSTEM (TO BE SOLD AS PEIOLASE FOR LASERENAP)
- K961163 — LARES RESEARCH AS-1 LOWSPEED HANDPIECE
- K905542 — LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS
- K905543 — LARES APOLLO CS/CP/C
- K905541 — LARES 757 WORKHORSE HIGHSPEED HANDPIECE
Data sourced from openFDA. This site is unofficial and independent of the FDA.