FDA applicant

Surgipro, Inc.

Palm Florida, FL5 decisions1993–19940 recalls

FDA records 5 decisions for Surgipro, Inc. (Palm Florida, FL) from 1993 to 1994: 5 510(k) clearances. Most are in product codes LRO (General Surgery Tray) and FRG (Wrap, Sterilization). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Surgipro, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Surgipro, 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 “Surgipro”

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

Surgipro Central, Inc. 1

Surgipro, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Surgipro”