Heraeus Lasersonics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Heraeus Lasersonics, Inc. - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
Heraeus Lasersonics, Inc. has 38 FDA 510(k) cleared general & plastic surgery devices. Based in Santa Clara, US.
Historical record: 38 cleared submissions from 1988 to 1994.
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.
FDA 510(k) Regulatory Record - Heraeus Lasersonics, Inc.
38 devices
Cleared
Apr 21, 1994
ULTRALINE II STERILE DISPOSABLE FIBER
General & Plastic Surgery
293d
Cleared
Nov 25, 1992
HERCULES MODEL 5060 AND 5100 ND:YAG LASER SYSTEMS
General & Plastic Surgery
113d
Cleared
Jun 18, 1992
ULTRALINE STERILE DISPOSABLE FIBER
General & Plastic Surgery
64d
Cleared
Jun 15, 1992
ND
General & Plastic Surgery
185d
Cleared
Mar 27, 1992
CO2 LASER AND WAVEGUIDE DELIVERY SYSTEMS FOR THOR.
General & Plastic Surgery
105d
Cleared
Feb 27, 1992
LASER SYSTEMS FOR PERCUTANEOUS LUMBAR DISCECTOMY
General & Plastic Surgery
259d
Cleared
Dec 09, 1991
C02 LASER WAVEGUIDE
General & Plastic Surgery
102d
Cleared
Oct 31, 1991
CARBON DIOXIDE LASER SYSTEMS W/WAVEGUIDE DELIVERY
General & Plastic Surgery
265d
Cleared
Sep 25, 1991
HERAEUS LASERSONICS TACTILASE STERILE DISPOS FIBER
General & Plastic Surgery
22d
Cleared
Sep 16, 1991
HERCULES 5000 AND HERCULES 5040 ND:YAG LASER SYSTE
General & Plastic Surgery
38d
Cleared
Sep 11, 1991
LATERALASE STERILE DISPOSABLE FIBER
General & Plastic Surgery
35d
Cleared
Aug 13, 1991
LUXUS 132 ND: YAG SURGICAL LASER SYSTEM
General & Plastic Surgery
99d
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