Beacon Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beacon Laboratories, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Beacon Laboratories, Inc. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Westminster, US.
Historical record: 18 cleared submissions from 1989 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 - Beacon Laboratories, Inc.
18 devices
Cleared
Mar 11, 1994
FLEXIBLE EXTENDER
General & Plastic Surgery
416d
Cleared
Jun 25, 1993
ARGON HANDPIECES
General & Plastic Surgery
144d
Cleared
Apr 20, 1993
DISPOSABLE ELECTROSURGERY BALL ELECTRODE
General & Plastic Surgery
159d
Cleared
Jan 15, 1993
SESQUIPOLAR(TM) MIS ELECTRODE
General & Plastic Surgery
245d
Cleared
Dec 24, 1992
DISPOSABLE HAND-SWITCHING ESU PENCIL
General & Plastic Surgery
48d
Cleared
Mar 13, 1992
MIS ELECTROSURGICAL ELECTRODES
General & Plastic Surgery
80d
Cleared
Feb 03, 1992
GSU HANDPIECE ADAPTER
General & Plastic Surgery
25d
Cleared
Nov 19, 1991
PRESSURE GUARD
General & Plastic Surgery
88d
Cleared
Jul 22, 1991
ARGON BEAM COMBO LAPAROSCOPIC ELECTRODE
General & Plastic Surgery
210d
Cleared
Dec 13, 1990
ACTIVE ADAPTER
General & Plastic Surgery
72d
Cleared
Nov 21, 1990
ARGON BEAM LAPAROSCOPIC ELECTRODE
General & Plastic Surgery
135d
Cleared
Sep 28, 1990
BEAMER 1,2,4,6, AND 8
General & Plastic Surgery
43d