FDA applicant

Interphase Implants, Inc.

Livonia, MI1 decision1990–19900 recalls

FDA records 1 decision for Interphase Implants, Inc. (Livonia, MI) in 1990: 1 510(k) clearance. All are in product code MDL (Implant, Transmandibular). 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 Interphase Implants, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Interphase Implants, 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

Interphase Implants, Inc.

Which product codes does it file in?

What has FDA decided for it lately?