# Surgikor, LLC

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 2 (2019–2024): 2 510(k) clearances
- Product codes: DZE (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Blue Sky Bio, LLC: 1 (https://510kreport.com/company/blue-sky-bio)
- Cortex Dental Implants Industries, Ltd.: 1 (https://510kreport.com/company/cortex-dental-implants-industries)

## Firms that cite its devices most
- Synoross Dba Osseone: 1 (https://510kreport.com/company/synoross-dba-osseone)
- Surcam Medical Devices and Developments, Ltd.: 1 (https://510kreport.com/company/surcam-medical-devices-and-developments)

## Its most-cited devices
- K182615: Surgikor Dental Implant System (2019), cited by 3

## Recent decisions
- K240803: Surgikor Fixation One, Abutment Blanks and Abutments (Sep 12, 2024)
- K182615: Surgikor Dental Implant System (Jul 8, 2019)

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