# Syn-Kit, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 34 (1980–1986): 34 510(k) clearances
- Product codes: JIL (11), DCN (2), DHR (2), KHE (2), JHJ (1), CEN (1), JXA (1), GMM (1), JHQ (1), GTQ (1), JJB (1), GMQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K861098: Seroiden Strepto Kit 'Eiken' (Aug 12, 1986)
- K861631: Slide Culture U 'Eiken' (Jun 10, 1986)
- K854819: CPR Slide Eiken (Feb 26, 1986)
- K854820: RA 80 Eiken (Jan 17, 1986)
- K853276: Aso Slide Eiken (Aug 20, 1985)
- K843754: Uropaper Eiken 7 (Dec 18, 1984)
- K843759: Uropaper Eiken Hag (Dec 18, 1984)
- K843757: Uropaper Eiken AG (Dec 18, 1984)

Source page: https://510kreport.com/company/syn-kit