Not currently registered with FDA under this name
Core-Vent Corp.
Las Vegas, NV, United States. Named as applicant on 25 dental 510(k) clearances between 1986 and 2000. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 251986–2000
- Markets registered in
- 22 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1980–2026
Registered in 2 markets
Where regulators' registries name Core-Vent Corp. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Core-Vent Corp. | 25 clearances | 1986–2000 | Below |
| Taiwan | TFDA | Manufacturer | CORE-VENT CORPORATION | 2 | 1991–1993 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
510(k) clearances
Clearances on which FDA names Core-Vent Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 8 Dec 2000 | K002614 | ADVENT IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 30 Oct 2000 | K002188 | SWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, SPB 8,10,12,14/OP3.5D/OPAR,OPB 8,10,12,14/OP2.3D/OP2.8D, | DZE Root-Form Endosseous Implant |
| 11 Jul 1995 | K950579 | MICRO-VENT IMPLANT | DZE Root-Form Endosseous Implant |
| 11 Jul 1995 | K950578 | SCREW-VENT IMPLANT | DZE Root-Form Endosseous Implant |
| 11 Jul 1995 | K950577 | SWEDE-VENT IMPLANT | DZE Root-Form Endosseous Implant |
| 11 Jul 1995 | K950576 | BIO-VENT X IMPLANT | DZE Root-Form Endosseous Implant |
| 11 Jul 1995 | K950575 | BIO-VENT IMPLANT | DZE Root-Form Endosseous Implant |
| 11 Feb 1992 | K912059 | PRE-ANGLED ABUTMENTS | DZE Root-Form Endosseous Implant |
| 30 Oct 1991 | K913782 | TCAL ABUTMENT | DZE Root-Form Endosseous Implant |
| 4 Oct 1991 | K910585 | TSIR ANGLED ABUTMENTS | DZE Root-Form Endosseous Implant |
| 15 May 1991 | K902968 | BIO-VENT-X ENDOSSEOUS HA COATED DENTAL IMPLANTS | DZE Root-Form Endosseous Implant |
| 20 Feb 1991 | K900181 | MICRO-VENT ENDOSSEOUS IMPLANT ABUTMENTS | DZE Root-Form Endosseous Implant |
| 20 Feb 1991 | K900179 | SCREW-VENT ENDOSSEOUS IMPLANT ABUTMENTS | DZE Root-Form Endosseous Implant |
| 19 Feb 1991 | K900180 | CORE-VENT ENDOSSEOUS IMPLANT ABUTMENTS | DZE Root-Form Endosseous Implant |
| 17 Dec 1990 | K902969 | SCREW-VENT ENDOSSEOUS HA COATED DENTAL IMPLANTS | DZE Root-Form Endosseous Implant |
| 9 Nov 1990 | K900634 | SWEDE-VENT ENDOSSEOUS HA COATED DENTAL IMPLANTS | DZE Root-Form Endosseous Implant |
| 9 Nov 1990 | K900182 | SWEDE-VENT ENDOSSEOUS IMPLANT ABUTMENTS | DZE Root-Form Endosseous Implant |
| 28 Jun 1990 | K900177 | CORE-VENT ARMENTARIUM | DZE Root-Form Endosseous Implant |
| 31 May 1990 | K900178 | ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES | EFS Oral Irrigation Unit |
| 1 Sep 1989 | K883717 | BIO-VENT | DZE Root-Form Endosseous Implant |
| 14 Mar 1988 | K873255 | THE MICRO-VENT/HA | DZE Root-Form Endosseous Implant |
| 26 Feb 1988 | K873818 | VENT CORP PIB IMPLANT | DZE Root-Form Endosseous Implant |
| 7 Jan 1987 | K864321 | MICRO-VENT | DZE Root-Form Endosseous Implant |
| 5 Nov 1986 | K861425 | SUB-VENT (TM) IMPLANT/ENDOSSEOUS BLADE IMPLANT | DZE Root-Form Endosseous Implant |
| 7 Oct 1986 | K861426 | SCREW-VENT (TM) IMPLANT/ENDOSSEOUS SCREW IMPLANT | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: ZimVie US Corp LLC (6), ARCH Medical Solutions - Escondido LLC (1).
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.