Ellman Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ellman Intl., Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Ellman Intl., Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Hewlett, US.
Historical record: 15 cleared submissions from 1996 to 2001.
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 - Ellman Intl., Inc.
15 devices
Cleared
Nov 07, 2001
SURGITRON 120 IEC (ALSO KNOWN AS SURGITRON 4.0 DUAL RF
General & Plastic Surgery
40d
Cleared
Apr 11, 2001
BIPOLAR TRIGGER-FLEX PROBE
General & Plastic Surgery
188d
Cleared
Sep 27, 2000
SURGITRON IEC II
General & Plastic Surgery
90d
Cleared
Jul 24, 2000
SURGITRON IEC II
General & Plastic Surgery
81d
Cleared
May 26, 2000
SURGITRON IEC II
General & Plastic Surgery
37d
Cleared
Oct 14, 1999
SURGITRON RADIOLASE
General & Plastic Surgery
90d
Cleared
Mar 17, 1999
SURGITRON
General & Plastic Surgery
57d
Cleared
Jul 07, 1998
SUGITRON MODEL: IEC
General & Plastic Surgery
168d
Cleared
Jun 29, 1998
SURGITRON
General & Plastic Surgery
160d
Cleared
Jun 19, 1997
SURGITRON MODEL FFPF-EMC
General & Plastic Surgery
16d
Cleared
Apr 15, 1996
DENTO-SURGE
Dental
154d
Cleared
Feb 29, 1996
ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGE
Obstetrics & Gynecology
139d