FDA applicant

Frontier Novelty, Inc.

Laredo, TX4 decisions1993–19940 recalls

FDA records 4 decisions for Frontier Novelty, Inc. (Laredo, TX) from 1993 to 1994: 4 510(k) clearances. 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 Frontier Novelty, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Frontier Novelty, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Frontier”

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

Frontier Medical Devices, Inc. 5 Frontier Products 4 Frontier Devices, Inc. 1

Frontier Novelty, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Frontier”