# Dynagen, Inc.

- Location (FDA's records): Cambridge, MA
- FDA decisions: 6 (1992–1996): 6 510(k) clearances
- Product codes: JSY (3), MIG (1), DIF (1), MRS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Lin-Zhi International, Inc.: 1 (https://510kreport.com/company/lin-zhi-international)

## Its most-cited devices
- K963733: Niccheck I (1996), cited by 1

## Recent decisions
- K963733: Niccheck I (Dec 13, 1996)
- K943051: Mycoakt M. Tuberculosis Cuulture ID Kit (Mar 13, 1995)
- K943049: Mycoakt M. Avium Culture ID Kit (Mar 13, 1995)
- K943050: Mycoakt M Kansasii Culture ID Kit (Mar 13, 1995)
- K931105: Procheck (TM) Blind Performance Specimens (Apr 21, 1993)
- K912888: Uritec Test Strip & Human Urine + & - Test Control (Feb 24, 1992)

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