FDA applicant

Inter-Pal GmbH

Palos Verdes Estates, CA1 decision1995–19950 recalls

FDA records 1 decision for Inter-Pal GmbH (Palos Verdes Estates, CA) in 1995: 1 510(k) clearance. All are in product code JAQ (System, Applicator, Radionuclide…). 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, radiology panel, where it files most

How often FDA has decided Inter-Pal GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inter-Pal GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inter-Pal GmbH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Inter-Pal”

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

Inter-Med, Inc. 12 Inter-Med/Vista Dental Products 6 Inter Medical Medizintechnik GmbH 3 Inter Med Industries, Inc. 3 Inter Science Institute 3 Inter-Os Technologies 2 Inter Continental Health Care 2 Inter-Asia Co., Inc. 1 Inter-Med / Vista Dental 1 Inter-Continental Industries Sdn Bhd 1

Inter-Pal GmbH

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Inter-Pal”