Medical Device Manufacturer · US , Denver , CO

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

10 submissions · 10 cleared · Since 1994

10

Total

10

Cleared

0

Denied

Optus, Inc. has 10 FDA 510(k) cleared medical devices. Based in Denver, US.

Historical record: 10 cleared submissions from 1994 to 1996.

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

Optus, 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 - Optus, Inc.

10 devices

1-10 of 10

Cleared Feb 02, 1996

OPTUS OTOSCOPES

Ear, Nose, Throat · 462d

Cleared Jan 22, 1996

OPTUS ARTHROSCOPE & MINI-ARTHROSCOPE ACCESSORIES

Orthopedic · 154d

Cleared Dec 21, 1995

OPTUS BRONCHOSCOPES

Ear, Nose, Throat · 419d

Cleared Sep 12, 1995

OPTUS HYSTEROSCOPES AND CONTACT HYSTEROSCOPES

Obstetrics & Gynecology · 319d

Cleared May 26, 1995

OPTUS CYSTOSCOPES AND PEDIATRIC CYSTOSCOPES

Gastroenterology & Urology · 210d

Cleared May 23, 1995

OPTUS ARTHROSCOPES AND MINI-ARTHROSCOPES

Orthopedic · 207d

Cleared Feb 23, 1995

OPTUS LAPAROSCOPES AND OPERATING LAPAROSCOPES

General & Plastic Surgery · 118d

Cleared Jan 26, 1995

OPTUS SINUSCOPES AND ACCESSORIES

Ear, Nose, Throat · 127d

Cleared Dec 13, 1994

OPTUS THORACOSCOPES

General & Plastic Surgery · 46d

Cleared Nov 07, 1994

OPTUS LARYNGOSCOPES

Anesthesiology · 10d