Not currently registered with FDA under this name

O Co., Inc.

Albuquerque, NM, United States. Named as applicant on 17 dental 510(k) clearances between 1989 and 2003. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
171989–2003
Markets registered in
1United States
Establishments
0—
1989: 11991: 11992: 21994: 11995: 51996: 11998: 12001: 12002: 32003: 119801990200020102020

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names O Co., Inc. as the applicant.

Decided510(k)DeviceDevice type
10 Dec 2003K033392IMMEDIATE STABILIZING IMPLANT (ISI)DZE Root-Form Endosseous Implant
9 Oct 2002K023336OCO DENTAL IMPLANT (5.0MM DIAMETER)DZE Root-Form Endosseous Implant
22 May 2002K021460OCO DENTAL IMPLANTNHA Endosseous Dental Implant Abutment
10 Apr 2002K011524IMMEDIATE STABILIZING DEVICE (ISD)DZE Root-Form Endosseous Implant
1 Feb 2001K010142OCO DENTAL IMPLANTDZE Root-Form Endosseous Implant
5 Jan 1998K973926O BUTMENT HS IMPLANTDZE Root-Form Endosseous Implant
15 Nov 1996K961665O BUTMENT ET IMPLANTDZE Root-Form Endosseous Implant
15 Sep 1995K950066DENTAL IMPLANT ENDOSSEOUSDZE Root-Form Endosseous Implant
1 Mar 1995K946129IMPLANT BODY DEPTH GAUGE/TRYINDZE Root-Form Endosseous Implant
1 Mar 1995K946113IMPLANT BODY RETRIEVER/REMOVERDZE Root-Form Endosseous Implant
16 Feb 1995K945300ACCESSORY ITEM TO ENDOSSEOUS DENTAL IMPLANTDZE Root-Form Endosseous Implant
16 Feb 1995K944904PARRALLEL PINDZE Root-Form Endosseous Implant
29 Aug 1994K923889O BUTMENT ES IMPLANTDZE Root-Form Endosseous Implant
8 Jul 1992K921933O BUTMENT HBDZE Root-Form Endosseous Implant
11 Feb 1992K903999OBUTMENT HBDZE Root-Form Endosseous Implant
29 Mar 1991K903211O BUTMENTDZE Root-Form Endosseous Implant
1 Aug 1989K884296O BUTMENTDZE Root-Form Endosseous Implant

Some of these clearances are listed with FDA today by another company: Oco Biomedical (2).

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.