FDA applicant

Continental Soft Lens, Inc.

Littleton, CO2 decisions1994–19990 recalls

FDA records 2 decisions for Continental Soft Lens, Inc. (Littleton, CO) from 1994 to 1999: 2 510(k) clearances. 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 Continental Soft Lens, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Continental Soft Lens, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Continental Soft Lens, 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 “Continental”

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

Continental X-Ray Corp. 27 Continental Medical Laboratories, Inc. 8 Continental Optical Imports 2 Continental Dental Laboratory 1 Continental Dental Ceramics, Inc. (Dba Continental 1 Continental Scale Corp. 1 Continental Dental Ceramics, Inc. 1 Continental Products, Inc. 1

Continental Soft Lens, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Continental”