510(k) Report

FDA applicant

FDC Technology Industry Co.

Kent, WA2 decisions2026–20260 recalls

FDA records 2 decisions for FDC Technology Industry Co. (Kent, WA) in 2026: 2 510(k) clearances. Most are in product codes EBW (Controller, Foot, Handpiece And Cord) and EFB (Handpiece, Air-Powered, Dental). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided FDC Technology Industry Co.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2026

2026 (partial year): 2
2026high 2 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

FIG. 1 — FDC Technology Industry Co. by year, 2026–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like FDC Technology Industry Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report