FDA applicant

Dalton Technology, Inc.

Glendale, CA2 decisions1990–19900 recalls

FDA records 2 decisions for Dalton Technology, Inc. (Glendale, CA) in 1990: 2 510(k) clearances. Most are in product codes HWE (Instrument, Surgical, Orthopedic, Ac-Powered…) and HXX (Screwdriver). 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, general and plastic surgery panel, where it files most

How often FDA has decided Dalton Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dalton Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dalton Technology, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “Dalton”

FDA records each applicant name separately; these may or may not be the same firm.

Dalton Medical Corp. 7 Dalton Instrument Corp. 5

Dalton Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dalton”