FDA applicant

Pioneer Intl. Co.

Hidden Hills, CA1 decision1990–19900 recalls

FDA records 1 decision for Pioneer Intl. Co. (Hidden Hills, CA) in 1990: 1 510(k) clearance. All are in product code FMF (Syringe, Piston). 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 Pioneer Intl. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pioneer Intl. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pioneer”

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

Pioneer Surgical Technology 77 Pioneer Surgical Technology, Inc. (Dba Rti Surgical… 16 Pioneer Viggo, Inc. 6 Pioneer Medical, Inc. 2 Pioneer Surgical Technology, Inc. (Rti Surgical, I 2 Pioneer Surgical Technology, Inc D.B.A Resolve… 2 Pioneer Sundries Products, Ltd. 2 Pioneer Trading Co. 1 Pioneer Surgical Technology, Inc. (Rti Surgical, Inc.) 1

Pioneer Intl. Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pioneer”