FDA applicant

Continental Scale Corp.

Bridgeview, IL1 decision1985–19850 recalls

FDA records 1 decision for Continental Scale Corp. (Bridgeview, IL) in 1985: 1 510(k) clearance. All are in product code FRW (Scale, Patient). 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, general hospital panel, where it files most

How often FDA has decided Continental Scale Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Continental Scale Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Continental Scale Corp. 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 Soft Lens, Inc. 2 Continental Optical Imports 2 Continental Dental Laboratory 1 Continental Dental Ceramics, Inc. (Dba Continental 1 Continental Dental Ceramics, Inc. 1 Continental Products, Inc. 1

Continental Scale Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Continental”