Geiger Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Geiger Medical Technologies, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Geiger Medical Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Monarch Beach, US.
Historical record: 5 cleared submissions from 1999 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Geiger Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Geiger Medical Technologies, Inc.
5 devices
Cleared
Oct 23, 2000
THERMAL CAUTERY UNIT, MODEL 150
Ophthalmic
83d
Cleared
May 23, 2000
GEIGER NEEDLE ADAPTER, MODEL 406
General & Plastic Surgery
54d
Cleared
Dec 27, 1999
GEIGER DISPOSABLE ELECTROSURGICAL ELECTRODE, MODEL 435
General & Plastic Surgery
25d
Cleared
Aug 19, 1999
GEIGER ELECTROSURGICAL HANDPIECE SHEATH, MODEL 405
General & Plastic Surgery
56d
Cleared
Jan 28, 1999
BLUE VALUE LINE OF ELECTROSURGICAL ELECTRODES, MODEL #'S 421-429
General & Plastic Surgery
90d