FDA applicant

Dalton Instrument Corp.

Addiison, TX5 decisions1985–20140 recalls

FDA records 5 decisions for Dalton Instrument Corp. (Addiison, TX) from 1985 to 2014: 5 510(k) clearances. Most are in product codes IOR (Wheelchair, Mechanical) and INO (Chair, Positioning, Electric). Its devices cite 3 predicates, 0 of them its own earlier devices. 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, physical medicine panel, where it files most

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

FDA decisions per year

1in 2014

2007high 2 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dalton Instrument Corp.’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

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 Technology, Inc. 2

Dalton Instrument Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Dalton”