FDA applicant

Pedia Pals, Inc.

Columbus, OH7 decisions1991–19950 recalls

FDA records 7 decisions for Pedia Pals, Inc. (Columbus, OH) from 1991 to 1995: 7 510(k) clearances. Most are in product codes DXQ (Blood Pressure Cuff) and ERA (Otoscope). 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, cardiovascular panel, where it files most

How often FDA has decided Pedia Pals, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pedia Pals, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pedia Pals, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Pedia”

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

Pedia, LLC 1

Pedia Pals, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pedia”