Heraeus Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Heraeus Surgical, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Heraeus Surgical, Inc. has 8 FDA 510(k) cleared medical devices. Based in Milpitas, US.
Historical record: 8 cleared submissions from 1994 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Heraeus Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Heraeus Surgical, Inc.
8 devices
Cleared
Aug 21, 1996
LASERSONICS ND:YAG CYLINDRICALLY DIFFUSING STERILE DISPOSABLE FIBER
General & Plastic Surgery
189d
Cleared
Feb 13, 1996
LASERSONICS PARASCAN DOSIMETER DEVICE
General & Plastic Surgery
57d
Cleared
Oct 26, 1995
LASESONICS LOW POWER CO2 LASER SYSTEM
General & Plastic Surgery
66d
Cleared
Apr 18, 1995
LASERSONICS ULTRALINE III STERILE DISPOSABLE FIBER
General & Plastic Surgery
32d
Cleared
Mar 14, 1995
LASERSONICS SURGICAL LASER SYSTEMS AND ACCESSORIES
General & Plastic Surgery
225d
Cleared
Nov 08, 1994
LASERSONICS RADIANCE DIODE LASER SYSTEMS AND ACCESSORIES
General & Plastic Surgery
63d
Cleared
Mar 23, 1994
LASERSONICS TISSUE MORCELLATOR SET
General & Plastic Surgery
124d
Cleared
Mar 01, 1994
LASERSONICS CLEARPULSE MODELS 50, 70 & 100 CO2 SURGICAL LASER SYSTEMS
General & Plastic Surgery
88d