FDA applicant

Radiant Spectacles Manufacturers

Baltimore, MD1 decision1994–19940 recalls

FDA records 1 decision for Radiant Spectacles Manufacturers (Baltimore, MD) in 1994: 1 510(k) clearance. All are in product code HQZ (Frame, Spectacle). 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 Radiant Spectacles Manufacturers’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Radiant Spectacles Manufacturers since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Radiant”

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

Radiant Innovation, Inc. 15 Radiant Medical 6 Radiant Express, LLC 1

Radiant Spectacles Manufacturers

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Radiant”