510(k) Report

FDA applicant

Surgical Implants, Inc.

Sarasota, FL1 decision2000–20000 recalls

FDA records 1 decision for Surgical Implants, Inc. (Sarasota, FL) in 2000: 1 510(k) clearance. All are in product code JDI (Prosthesis, Hip, Semi-Constrained…). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Surgical Implants, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Surgical Implants, 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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