Medical Device Manufacturer · US , Attleboro , MA

Ultracision, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1989

Total

Cleared

Denied

Ultracision, Inc. has 9 FDA 510(k) cleared medical devices. Based in Attleboro, US.

Historical record: 9 cleared submissions from 1989 to 1995. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Ultracision, Inc. Filter by specialty or product code using the sidebar.

Ultracision, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ultracision, Inc.

9 devices

1-9 of 9

Cleared Jun 23, 1995

ULTRACISION HARMONIC SCAPEL

K952726 · GEI

General & Plastic Surgery · 9d

Cleared Jul 01, 1994

ULTRACISON HARMONIC SCALPEL HS2 BLADE

K941897 · GEI

General & Plastic Surgery · 74d

Cleared Jun 08, 1993

HARMONIC SCALPEL REUSABLE LAPORASCOPIC BLADE SYST.

K930352 · GCJ

General & Plastic Surgery · 138d

Cleared May 21, 1993

HARMONIC SCALPEL 5MM LAPAROSONIC BLADE ACCESSORY

K924917 · GEI

General & Plastic Surgery · 234d

Cleared May 17, 1993

HARMONIC SCALPEL LAPAROSONIC CLAMP COAGULATOR ACC.

K925699 · GCJ

General & Plastic Surgery · 186d

Cleared Apr 23, 1993

HARMONIC SCALPEL LAPAROSONIC BLADE ACCESSORY

K924281 · GCJ

General & Plastic Surgery · 241d

Cleared Jun 24, 1991

HARMONIC SCALPEL ENDOSCOPIC BLADE COUPLER EXTENSIO

K911341 · GEI

General & Plastic Surgery · 90d

Cleared Feb 15, 1991

ULTRACISION HARMONIC SCALPEL

K905315 · GEI

General & Plastic Surgery · 79d

Cleared Oct 31, 1989

ULTRACISION ULTRASONIC SCALPEL

K895252 · GEI

General & Plastic Surgery · 71d

Ultracision, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Ultracision, Inc.

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