Medical Device Manufacturer · US , Moultonboro , NH

Portlyn Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1990

8

Total

8

Cleared

0

Denied

Portlyn Corp. has 8 FDA 510(k) cleared medical devices. Based in Moultonboro, US.

Historical record: 8 cleared submissions from 1990 to 1997.

Browse the FDA 510(k) cleared devices submitted by Portlyn Corp. Filter by specialty or product code using the sidebar.

Portlyn Corp. 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 - Portlyn Corp.

8 devices

1-8 of 8

Cleared Jun 17, 1997

DYNABITE HOT GI BIOPSY FORCEPS

Gastroenterology & Urology · 159d

Cleared Jul 27, 1995

DYNABITE CARDIOVASCULAR BIOPSY FORCEPS

Cardiovascular · 120d

Cleared Jun 01, 1995

DYNABITE UROLOGICAL FORCEPS

Gastroenterology & Urology · 10d

Cleared Nov 15, 1994

DYNABITE LAPAROSCOPIC FORCEPS

Obstetrics & Gynecology · 77d

Cleared Mar 22, 1994

DYNABITE HYSTEROSCOPIC FORCEPS

Obstetrics & Gynecology · 189d

Cleared Jun 29, 1990

Cardiovascular · 101d

Cleared Apr 16, 1990

BIOPSY FORCEP (NON-ELECTRIC)

Gastroenterology & Urology · 175d

Cleared Mar 09, 1990

BIOPSY FORCEPS, (NON-RIGID)

Ear, Nose, Throat · 137d