Ergo Intl., Ent., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ergo Intl., Ent., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Ergo Intl., Ent., Inc. has 5 FDA 510(k) cleared medical devices. Based in North Miami Beach, US.
Historical record: 5 cleared submissions from 1988 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ergo Intl., Ent., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ergo Intl., Ent., Inc.
5 devices
Cleared
Jul 14, 1989
NON-STERILE PATIENT EXAM GLOVES (LATEX)
General Hospital
100d
Cleared
May 25, 1989
PROLAX PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
56d
Cleared
May 08, 1989
PATIENT EXAM GLOVES (MFG. SHUN JUN TRADING CO.)
General Hospital
35d
Cleared
May 08, 1989
PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES)
General Hospital
35d
Cleared
Nov 07, 1988
ERGO II, SURGICAL LATEX GLOVES
General Hospital
45d