Fort Defiance Industries, LLC
Fort Defiance Industries, LLC holds FDA 510(k) medical device clearances, first cleared 2022, most recent 2025, with 3 FDA device recalls on record.
Top product codes for Fort Defiance Industries, LLC
FDA recalls by Fort Defiance Industries, LLC
- Z-2983-2026 — Fort Defiance Industries (FDI), Automated Field Steam Sterilizer REF: P2131
- Z-0121-2022 — P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641
- Z-2411-2018 — FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER, NSN: 6530-01-641-4641 Product Usage: The Fort Defiance Industries Automated Field Steam Sterilizer Model P2131 is designed for sterilization of porous and non-porous, heat- and moisture-stable materials (e.g., surgical instruments and textiles) used in healthcare facilities. The P2131 sterilizer is a transportable device designed for use in a variety of austere environments.
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 Fort Defiance Industries, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.