Laser Peripherals, LLC - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Laser Peripherals, LLC has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Hingham, US.
Historical record: 12 cleared submissions from 1988 to 2017.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
12 devices
Cleared
Jun 08, 2017
Laser Peripherals, LLC Family of Bare Laser Fibers
General & Plastic Surgery
122d
Cleared
Apr 25, 2003
BARE LASER FIBER MODELS DBLF-40, DBLF-60, DBLF-60-1, DCLF-600B, DSLF-60,...
General & Plastic Surgery
29d
Cleared
Jul 24, 2001
LASER PERIPHERALS REUSABLE HOLMIUM FIBER
General & Plastic Surgery
96d
Cleared
Jul 12, 1999
SCATTERFREE LATERAL EMITTING FIBER
General & Plastic Surgery
21d
Cleared
Feb 10, 1998
LS-905 FIBERCHOICE ADAPTER SYSTEM
General & Plastic Surgery
90d
Cleared
Jul 29, 1997
LASER PERIPHERALS HOLMIUM BARE FIBERS
General & Plastic Surgery
41d
Cleared
Jun 27, 1996
LASER PERIPHERALS INC. BARE FIBER
General & Plastic Surgery
66d
Cleared
May 22, 1996
LASER PERIPHERALS INC. SCATTERFREE FIBER
General & Plastic Surgery
65d
Cleared
Jun 27, 1990
LASEGUIDE CAT # CLF-600D & CLF-1000D
General & Plastic Surgery
70d
Cleared
Jun 01, 1988
LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE
Obstetrics & Gynecology
111d
Cleared
Apr 25, 1988
LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE
Anesthesiology
74d
Cleared
Mar 23, 1988
LASEGUIDE 600A, 600B, 400A, AND 400B
Gastroenterology & Urology
131d