Dynex Technologies, Inc.
Dynex Technologies, Inc. holds FDA 510(k) medical device clearance, cleared in 2023, with 2 FDA device recalls on record.
Top product codes for Dynex Technologies, Inc.
FDA recalls by Dynex Technologies, Inc.
- Z-2345-2025 — Dynex Agility Sample Tips; Model Number: 67910; The 67910 Agility Sample Tips are an accessory/consumable used with the Agility Automated ELISA system.
- Z-1222-2022 — DYNEX Agility, Agility Analyzer, Model No. 67000
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Dynex Technologies, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.