# Core-Vent Corp.

- Location (FDA's records): Encino, CA
- FDA decisions: 25 (1986–2000): 25 510(k) clearances
- Product codes: DZE (24), EFS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- O Co., Inc.: 2 (https://510kreport.com/company/o)
- Almitech, Inc.: 2 (https://510kreport.com/company/almitech)
- Zimmer Dental, Inc.: 2 (https://510kreport.com/company/zimmer-dental)
- Crystal Medical Technology: 1 (https://510kreport.com/company/crystal-medical-technology)
- Alpha-Bio Tec, Ltd.: 1 (https://510kreport.com/company/alpha-bio-tec)
- Osstem Co., Ltd.: 1 (https://510kreport.com/company/osstem)
- Quantum Bioengineering, Ltd.: 1 (https://510kreport.com/company/quantum-bioengineering)
- Dentatus USA, Ltd.: 1 (https://510kreport.com/company/dentatus-usa)

## Its most-cited devices
- K861426: Screw-Vent (TM) Implant/Endosseous Screw Implant (1986), cited by 4
- K900179: Screw-Vent Endosseous Implant Abutments (1991), cited by 2
- 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, (2000), cited by 2
- K950577: Swede-Vent Implant (1995), cited by 1
- K002614: Advent Implant System (2000), cited by 1
- K950578: Screw-Vent Implant (1995), cited by 1

## Recent decisions
- K002614: Advent Implant System (Dec 8, 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, (Oct 30, 2000)
- K950575: Bio-Vent Implant (Jul 11, 1995)
- K950577: Swede-Vent Implant (Jul 11, 1995)
- K950579: Micro-Vent Implant (Jul 11, 1995)
- K950576: Bio-Vent X Implant (Jul 11, 1995)
- K950578: Screw-Vent Implant (Jul 11, 1995)
- K912059: Pre-Angled Abutments (Feb 11, 1992)

Source page: https://510kreport.com/company/core-vent