Medical Device Manufacturer · US , Hewlett , NY

Ellman Intl., Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1996

15

Total

15

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ellman Intl., Inc. General & Plastic Surgery ✕

12 devices

1-12 of 12

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

General & Plastic Surgery · 57d

Cleared Jul 07, 1998

SUGITRON MODEL: IEC

General & Plastic Surgery · 168d

Cleared Jun 29, 1998

General & Plastic Surgery · 160d

Cleared Jun 19, 1997

SURGITRON MODEL FFPF-EMC

General & Plastic Surgery · 16d

Cleared Feb 08, 1996

General & Plastic Surgery · 119d

Cleared Feb 08, 1996

General & Plastic Surgery · 87d