Candela Laser Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Candela Laser Corp. - FDA 510(k) Cleared Devices
43
Total
43
Cleared
0
Denied
Candela Laser Corp. has 43 FDA 510(k) cleared medical devices. Based in Wayland, US.
Historical record: 43 cleared submissions from 1988 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Candela Laser Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Candela Laser Corp.
43 devices
Cleared
Aug 15, 1996
ANDELA DYNAMIC COOLING DEVICE
Physical Medicine
528d
Cleared
Jun 14, 1996
CANDELA Q-SWITCHED ALEXANDRITE LASERS
General & Plastic Surgery
185d
Cleared
Apr 03, 1996
CANDELA HCS 2000 URETHERAL WARMER CATHETER
General & Plastic Surgery
154d
Cleared
Feb 05, 1996
CANDELA CRYO-PROBE HOLDER
General & Plastic Surgery
104d
Cleared
Feb 02, 1996
CANDELA SPTL LONG PULSE/TUNABLE PULSED DYE LASE
General & Plastic Surgery
98d
Cleared
Oct 24, 1995
CANDELA MODEL PLTL-1 LASER SYSTEM
General & Plastic Surgery
96d
Cleared
Oct 18, 1995
CANDELA CRYOSYSTEM CS-5
General & Plastic Surgery
96d
Cleared
May 26, 1995
ALEXLAZR
General & Plastic Surgery
91d
Cleared
Mar 24, 1995
CANDELA RUBY LAZE Q-SWITCHED RUBY LASER
General & Plastic Surgery
93d
Cleared
Mar 10, 1995
CANDELA 10MM CIRCULAR SPOT LASER HANDPIECE
General & Plastic Surgery
25d
Cleared
Mar 09, 1995
CANDELA SPTL VARIABLE PULSE/TUNABLE PULSED DYE LASERS
General & Plastic Surgery
244d
Cleared
Mar 06, 1995
CANDELA URETHRAL/BLADDER SOUND
Gastroenterology & Urology
21d
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