Medical Device Manufacturer · US , Gainsville , FL

Medical Device Technologies, Inc. - FDA 510(k) Cleared Devices

46 submissions · 46 cleared · Since 1992

Recent clearances: BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT, INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR, INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR

Total

Cleared

Denied

Medical Device Technologies, Inc. has 46 FDA 510(k) cleared medical devices. Based in Gainsville, US.

Historical record: 46 cleared submissions from 1992 to 2010. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by Entela, Inc. as regulatory consultant.

Medical Device Technologies, Inc. is one of 13072 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medical Device Technologies, Inc.

46 devices

1-12 of 46

Cleared Aug 27, 2010

BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT

K101832 · KNW

Gastroenterology & Urology · 57d

Cleared Jan 26, 2006

INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR

K053518 · NEU

General & Plastic Surgery · 38d

Cleared Aug 30, 2005

INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR

K051421 · NEU

General & Plastic Surgery · 90d

Cleared May 26, 2005

CANALIZER HYDROPHILIC GUIDE WIRE

K050873 · DQX

Cardiovascular · 50d

Cleared Feb 11, 2005

INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE

K043523 · KNW

Gastroenterology & Urology · 53d

Cleared Sep 30, 2004

V-CORE FULL CORE BREAST BIOPSY INSTRUMENT

K042464 · KNW

Gastroenterology & Urology · 17d

Cleared May 03, 2004

FIBREX CATHETER PATENCY DEVICE

K040427 · FOZ

General Hospital · 74d

EN-SNARE ENDOVASCULAR SNARE AND CATHETER

K021606 · MMX

Cardiovascular · 15d

Cleared Sep 05, 2001

MICROCRUISER PLUS INTRODUCER SET

K011790 · DYB

Cardiovascular · 89d

Cleared Oct 30, 2000

PBN FALLOPIAN TUBE CATHETER SYSTEM

K000620 · MDG

Obstetrics & Gynecology · 249d

Cleared Sep 11, 2000

GOLDEN-RULE SCALING CATHETER

K002416 · DQO

Cardiovascular · 34d

Looking for a specific device from Medical Device...? Search by device name or K-number.

Search all Medical Device... devices

Medical Device Technologies, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Medical Device Technologies, Inc.

Filters