FDA applicant

Specialty Tint

Front Royal, VA1 decision2000–20000 recalls

FDA records 1 decision for Specialty Tint (Front Royal, VA) in 2000: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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 Specialty Tint’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Specialty Tint since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Specialty”

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

Specialty Surgical Products, Inc. 13 Specialty Ultravision, Inc. 12 Specialty Packaging Producs, Inc. 11 Specialty Medical Products Co. 4 Specialty Appliance Works, Inc. 3 Specialty Medical Industries, Inc. 3 Specialty Water Technologies 2 Specialty Spine Products, LLC 2 Specialty Fibres and Materials, Ltd. 2 Specialty Health Products, Inc. 2 Specialty Dialysis Services 1 Specialty Drives Technologies, Inc. 1

Specialty Tint

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Specialty”