Medical Device Manufacturer · US , Albuquerque , NM

"O" Co., Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1989

Total

Cleared

Denied

"O" Co., Inc. has 17 FDA 510(k) cleared dental devices. Based in Albuquerque, US.

Historical record: 17 cleared submissions from 1989 to 2003.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

"O" Co., 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 - "O" Co., Inc.

17 devices

1-17 of 17

Cleared Dec 10, 2003

IMMEDIATE STABILIZING IMPLANT (ISI)

K033392 · DZE

Dental · 48d

Cleared Oct 09, 2002

OCO DENTAL IMPLANT (5.0MM DIAMETER)

IMMEDIATE STABILIZING DEVICE (ISD)

DENTAL IMPLANT ENDOSSEOUS

K950066 · DZE

Dental · 249d

Cleared Mar 01, 1995

IMPLANT BODY RETRIEVER/REMOVER

K946113 · DZE

Dental · 76d

Cleared Mar 01, 1995

IMPLANT BODY DEPTH GAUGE/TRYIN

ACCESSORY ITEM TO ENDOSSEOUS DENTAL IMPLANT

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026

"O" Co., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - "O" Co., Inc.

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