FDA applicant

Martin Dalsing

Grand Junction, CO2 decisions1997–19970 recalls

FDA records 2 decisions for Martin Dalsing (Grand Junction, CO) in 1997: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 1 predicate, 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, ophthalmic panel, where it files most

How often FDA has decided Martin Dalsing’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Martin Dalsing since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Martin Dalsing’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 “Martin”

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

Martin Medical 14 Martin'S Maine Exchange 4 Martin Uram, MD 2 Martin S. Knopf Assoc., Inc. 2 Martin E. Wendelken 1 Martin A. Hass, D.D.S. 1 Martin D. Lerman 1 Martin Manufacturing Co., LLC 1 Martin Mclane Medical 1 Martin H. Kaufmann 1 Martin Electric Co. 1 Martin Pelvic Lift Co. 1

Martin Dalsing

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Martin”