Candela Corp.
Candela Corp. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2019.
Top product codes for Candela Corp.
Recent clearances by Candela Corp.
- K183452 — Vbeam Prima Laser System
- K140732 — CANDELA GENTLELASE FAMILY OF LASER SYSTEMS
- K140122 — CANDELA GENTLEMAX FAMILY OF LASER SYSTEM
- K133283 — CANDELA GENTLEMAX FAMILY OF LASER SYSTEMS
- K112715 — CANDELA GENTLEMAX FAMILY OF LASERS
- K111144 — CANDELA GENTLELASE FAMILY OF LASERS
- K081324 — CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASERS
- K073534 — CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS
- K071469 — INOLASE SERENITY PSF ( PNEUMATIC SKIN FLATTENING) SYSTEM
- K063800 — CANDELA FLUORESCENT PULSED LIGHT SYSTEM
- K063074 — CANDELA 3630 LASER SYSTEM
- K063072 — CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS: 532 AND 1064 ND:YAG HANDPIECE ACCESSORIES
- K063073 — CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS
- K051359 — CANDELA FAMILY OF PULSED DYE LASER SYSTEMS: PIGMENTED LESION HANDPIECE ACCESSORY
- K050673 — CANDELA FAMILY OF PULSE DYE LASER SYSTEMS
- K043251 — CANDELA FAMILY OF PULSED DYE LASER SYSTEMS, MODELS VBEAM, CBEAM, SPTL-1B
- K041242 — CANDELA SMOOTHBEAM LASER SYSTEM
- K033331 — CANDELA CBEAM PULSE DYE LASER SYSTEM
- K033461 — CANDELA VBEAM PULSE DYE LASER SYSTEM
- K030834 — CANDELA SMOOTHBEAM LASER SYSTEM
- K033172 — CANDELA GENTLEYAG FAMILY OF LASER SYSTEMS
- K030846 — CANDELA SMOOTHBEAM LASER SYSTEM
- K024371 — CANDELA GENTLE LASE FAMILY OF LASER SYSTEM
- K024260 — CANDELA GENTLELASE FAMILY OF LASER SYSTEMS
- K022923 — CANDELA GENTLE YAG LASER SYSTEM
- K024335 — CANDELA GENTLELASE FAMILY OF LASER SYSTEMS
- K022951 — CANDELA GENTLE YAG LASER SYSTEM, VARIABLE PULSE YAG
- K022884 — CANDELA SMOOTHBEAM LASER SYSTEM
- K023193 — CANDELA GENTLE YAG LASER SYSTEM
- K014128 — CANDELA SMOOTHBEAM LASER SYSTEM
- K021180 — CANDELA VBEAM PULSED DYE LASER SYSTEM
- K020958 — CANDELA CBEAM PULSED DYE LASER SYSTEM
- K013825 — CANDELA SMOOTHBEAM LASER SYSTEM
- K013748 — CANDELA SCLERO LONG PULSE LASER (AKA VBEAM)
- K013043 — CANDELA CLEARBEAM PULSED DYE LASER
- K011092 — CANDELA SPTL-1E PULSED DYE LASER
- K010104 — CANDELA LONG PULSE ND:YAG
- K002421 — CANDELA MID IR DIODE LASER SYSTEM
- K001093 — CANDELA SPTL-1B PULSED DYE LASER
- K001589 — CANDELA DYNAMIC COOLING DEVICE
- K994260 — CANDELA GENTLELASE GL DERMATOLOGICAL LASER
- K993671 — CANDELA SCLERO LONG PULSE DYE LASER
- K984601 — CANDELA GENTLELASE II DERMATOLOGICAL LASER
- K981351 — CANDELA GENTLELASE GL DERMATOLOGICAL LASER
- K974381 — CANDELA GENTLELASE GL DERMATOLOGICAL LASER
- K972767 — CANDELA GENTLELASE GL DERMATOLOGICAL VASCULAR LESION LASER
- K863642 — CANDELA MODEL MDL-1 LASER LITHOTRIPTOR
- K861179 — CANDELA MODEL SPT-1, PULSED DYE LASER
Data sourced from openFDA. This site is unofficial and independent of the FDA.