# Berkley and Co.

- Location (FDA's records): Spirit Lake, IA
- FDA decisions: 3 (1984–1985): 3 510(k) clearances
- Product codes: DZC (2), GAA (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
- K854579: Hypodermic Needle and Stylet (Dec 17, 1985)
- K843171: Filafex TM, Esthetic Orthodontic Wire (Dec 3, 1984)
- K833788: Filafex Esthetic Orthodinic Wire (Jan 24, 1984)

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