FDA applicant

Implant Integration Systems, Inc.

Paradise, CA4 decisions1995–19980 recalls

FDA records 4 decisions for Implant Integration Systems, Inc. (Paradise, CA) from 1995 to 1998: 4 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 11 predicates, 0 of them its own earlier devices. 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Implant Integration Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Implant Integration Systems, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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 Logistics, Inc. 3 Implant Corp. of America 3 Implant Solutions Pty Ltd (Aka Osteon Medical) 2

Implant Integration Systems, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Implant”