FDA applicant

Flexible Dimensions, LLC

Lake Forest, CA1 decision2000–20000 recalls

FDA records 1 decision for Flexible Dimensions, LLC (Lake Forest, CA) in 2000: 1 510(k) clearance. All are in product code EBG (Crown And Bridge, Temporary, Resin). 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, dental panel, where it files most

How often FDA has decided Flexible Dimensions, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Flexible Dimensions, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Flexible”

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

Flexible Stenting Solutions, Inc. 5

Flexible Dimensions, LLC

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Flexible”