Medical Device Manufacturer · US , San Antonio , TX

Biomedical Ent., Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1996

Total

Cleared

Denied

Biomedical Ent., Inc. has 13 FDA 510(k) cleared medical devices. Based in San Antonio, US.

Historical record: 13 cleared submissions from 1996 to 2014. Primary specialty: Orthopedic.

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

Biomedical Ent., 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 - Biomedical Ent., Inc.

13 devices

1-13 of 13

SMOOTH OR THREADED METALLIC BONE FASTENER

MEMOGRAPH STAPLE, WARM SYSTEM

K993714 · JDR

Orthopedic · 115d

Cleared Jul 29, 1997

BONE AND MARROW COLLECTION SYSTEM KIT

K971782 · GEY

General & Plastic Surgery · 76d

Cleared Nov 14, 1996

BME BONE DRILL BITS

K964073 · GEY

General & Plastic Surgery · 34d

Cleared Aug 06, 1996

BONE & MARROW COLLECTION SYSTEM

K961901 · GEY

General & Plastic Surgery · 82d

Biomedical Ent., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Biomedical Ent., Inc.

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