# Syntex Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 10 (1976–1992): 10 510(k) clearances
- Product codes: JAK (4), EJJ (1), HRQ (1), EAY (1), EFB (1), DYN (1), DIS (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
- K920314: Txit D.a.U. Barbiturate Assay (Modification) (Apr 17, 1992)
- K843593: Surgipress Surgical Loop (Oct 24, 1984)
- K780997: Amalgam Alloy (Jul 27, 1978)
- K780769: S-100 CT Scanner (Jun 2, 1978)
- K780483: Fiber Optic Handpiece (Apr 28, 1978)
- K761331: Opus I Option - Fiber Optic L System (Jan 3, 1977)
- K761330: Syntex System 6000 (Dec 30, 1976)
- K761332: HI-Sensitivity Mode Option for S60-1A (Dec 30, 1976)

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