# Imcor

- Location (FDA's records): Edina, MN
- FDA decisions: 7 (1996–1999): 7 510(k) clearances
- Product codes: DZE (7)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Lifecore Biomedical, Inc.: 1 (https://510kreport.com/company/lifecore-biomedical)
- BioHorizons Implant Systems, Inc.: 1 (https://510kreport.com/company/biohorizons-implant-systems)
- O Co., Inc.: 1 (https://510kreport.com/company/o)

## Its most-cited devices
- K992512: Altiva Corporation NTR 3.3 MM Self-Tapping Screw Implants, Altiva Corporation Corporation NTR-3.3 MM Self-Tapping HA Coa (1999), cited by 3

## Recent decisions
- K992512: Altiva Corporation NTR 3.3 MM Self-Tapping Screw Implants, Altiva Corporation Corporation NTR-3.3 MM Self-Tapping HA Coa (Nov 1, 1999)
- K983563: Imcor 4.00 & 5.00MM Self-Tapping Locktite Implants, Imcor 4.00 & 5.00MM Self-Tapping HA Coasted Locktite Implants, and I (Jan 11, 1999)
- K982492: Imcor Dental Implant System Accessories (Oct 15, 1998)
- K974126: Imcor 3.75 and 5.00MM Externally Hexed, Self Tapping HA Coated Screw Implants with Cover Screw (Jan 30, 1998)
- K973049: Imcor Externally Hexed, Self-Tapping Screw Implant Surgical Drilling System (Nov 13, 1997)
- K960899: Imcor 5.00 MM Hex Self-Tapping Screw W/Cover Screw (Jun 17, 1996)
- K960900: Imcor 3.75 MM Wide Hex Self-Tapping Screw W/Cover Screw (Jun 5, 1996)

Source page: https://510kreport.com/company/imcor