Alm Surgical Equipment, Inc. is one of 15106 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alm Surgical Equipment, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ALM PRISMALIX (PRX) SURGICAL LIGHT, DRAGER GEMINA WALL-MOUNTED WORKPLACE, DRAGER DVE 8080/81/82 WITH DVE 4002 OR DVE 4001 SERIES SYSTEM
10
Total
10
Cleared
0
Denied
Alm Surgical Equipment, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Pasadena, US.
Historical record: 10 cleared submissions from 1988 to 1998.
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 - Alm Surgical Equipment, Inc.
10 devices
Cleared
Sep 22, 1998
ALM PRISMALIX (PRX) SURGICAL LIGHT
General & Plastic Surgery
102d
Cleared
Jul 30, 1996
DRAGER GEMINA WALL-MOUNTED WORKPLACE
General & Plastic Surgery
76d
Cleared
Jul 26, 1996
DRAGER DVE 8080/81/82 WITH DVE 4002 OR DVE 4001 SERIES SYSTEM
General & Plastic Surgery
81d
Cleared
Nov 04, 1994
MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE
Gastroenterology & Urology
17d
Cleared
Jul 13, 1994
DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032E
General & Plastic Surgery
76d
Cleared
Jan 12, 1993
ALM ILLUMINATOR SERIES LIGHT SYSTEM
General & Plastic Surgery
236d
Cleared
Nov 27, 1992
DRAGER DVE 4000 SERIES SYSTEM
General & Plastic Surgery
255d
Cleared
Oct 01, 1992
BFW WEHMERLITE IV-A FIBER OPTIC SURG. HEADLIGHT
General & Plastic Surgery
167d
Cleared
Oct 13, 1988
ALM OPERATING TABLES
General & Plastic Surgery
21d
Cleared
Jul 18, 1988
ALM SURGICAL LAMPS
General & Plastic Surgery
24d