FDA applicant

Implant Resource, Inc.

Prior Lake, MN2 decisions1997–20000 recalls

FDA records 2 decisions for Implant Resource, Inc. (Prior Lake, MN) from 1997 to 2000: 2 510(k) clearances. Most are in product codes HTY (Pin, Fixation, Smooth) and KIJ (Instrument, Surgical, Orthopedic, Dc-Powered…). 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 Implant Resource, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Implant Resource, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Implant Resource, 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 “Implant”

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

Implant Innovations, Inc. 51 Implant Center of the Palm Beaches 32 Implant Innovations International, Inc. 18 Implant Direct Sybron Manufacturing, LLC 17 Implant Technology, Inc. 13 Implant Support Systems, Inc. 10 Implant Direct, LLC 10 Implant Protesis Dental 2004, S.L. 6 Implant Sciences Corp. 6 Implant Integration Systems, Inc. 4 Implant Logistics, Inc. 3 Implant Corp. of America 3

Implant Resource, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Implant”