FDA applicant

Crystal Reflections, Int., Inc.

Front Royal, VA1 decision2000–20000 recalls

FDA records 1 decision for Crystal Reflections, Int., Inc. (Front Royal, VA) in 2000: 1 510(k) clearance. 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 Crystal Reflections, Int., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Crystal Reflections, Int., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Crystal Reflections, Int., 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 “Crystal”

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

Crystal Medical Products, Inc. 5 Crystal Diagnostics, Inc. 2 Crystal Medical Technology 2 Crystal Optical Co., Ltd. 1 Crystal Care Intl., Inc. 1 Crystal Tone Hearing Instruments 1 Crystal Medtech, LLC 1 Crystal Mark, Inc. 1 Crystal-Seal Dental Implants 1

Crystal Reflections, Int., Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Crystal”