Medical Device Manufacturer · US , Bloomfield , IN

Mectra Labs, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1992

Total

Cleared

Denied

Mectra Labs, Inc. has 9 FDA 510(k) cleared medical devices. Based in Bloomfield, US.

Historical record: 9 cleared submissions from 1992 to 2012. Primary specialty: Obstetrics & Gynecology.

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

Mectra Labs, 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 - Mectra Labs, Inc.

9 devices

1-9 of 9

Cleared Jun 29, 2012

TUBALGATOR

K113080 · HIN

Obstetrics & Gynecology · 255d

Cleared Mar 10, 2004

ELECTRO-LUBE

K033880 · GEI

General & Plastic Surgery · 86d

Cleared Nov 08, 2002

PNEUMOPERITONEUM INSUFFLATION NEEDLE

K021247 · HIF

Obstetrics & Gynecology · 203d

Cleared Mar 03, 2000

ENDOSCOPIC ANTI FOG DEVICE

K993604 · OCT

Gastroenterology & Urology · 130d

Cleared Apr 05, 1996

SUCTION CAUTERY PROBE

K955352 · GEI

General & Plastic Surgery · 136d

Cleared Feb 18, 1994

MECTRA TROCAR

K934547 · GCJ

General & Plastic Surgery · 149d

Cleared Feb 15, 1994

GRASPERS

K935382 · GCJ

General & Plastic Surgery · 99d

Cleared Sep 23, 1993

INSUFFLATION TUBING

K925691 · HIF

Obstetrics & Gynecology · 315d

Cleared Jul 13, 1992

INSUFFLATOR, LAPAROSCOPIC

K920959 · HIF

Obstetrics & Gynecology · 139d

Mectra Labs, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Mectra Labs, Inc.

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