New England Surgical Instrument Corp. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
New England Surgical Instrument Corp. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Walker, US.
Historical record: 18 cleared submissions from 1981 to 1989.
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.
18 devices
Cleared
Sep 15, 1989
ELECTROSURGICAL ELECTRODE
General & Plastic Surgery
16d
Cleared
Sep 15, 1989
ELECTROSURGICAL COAGULATION SUCTION TUBE
General & Plastic Surgery
16d
Cleared
Oct 07, 1988
RANEY AND LEROY-RANEY SCALP CLIP
Neurology
17d
Cleared
Sep 13, 1988
HANDSWITCHING MONOPOLAR PENCIL
General & Plastic Surgery
33d
Cleared
Apr 19, 1988
BIPOLAR MICRO COAGULATOR MODELS 25-1000 & 25-1200
General & Plastic Surgery
49d
Cleared
Mar 21, 1988
SURGICAL BURS
General & Plastic Surgery
20d
Cleared
Jun 26, 1987
VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS
General & Plastic Surgery
14d
Cleared
Jun 23, 1987
ARTHROPLASTY MALLET
General & Plastic Surgery
14d
Cleared
Feb 24, 1987
SUCTION TUBE
Gastroenterology & Urology
81d
Cleared
Feb 12, 1987
CHISEL (OSTEOTOME, GOUGE, ETC.)
Dental
69d
Cleared
Feb 04, 1987
CHUCK HANDLE
General & Plastic Surgery
61d
Cleared
Jan 20, 1987
BIPOLAR ELECTROSURGICAL INTRAOCULAR PROBE
General & Plastic Surgery
75d