510(k) Report

FDA applicant

Implant Center of the Palm Beaches

N. Palm Beach, FL32 decisions1994–19980 recalls

FDA records 32 decisions for Implant Center of the Palm Beaches (N. Palm Beach, FL) from 1994 to 1998: 32 510(k) clearances. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 30 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “The Implant Center of the Palm Beaches”.

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 Center of the Palm Beaches’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Implant Center of the Palm Beaches since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Implant Center of the Palm Beaches by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Implant Center of the Palm Beaches’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.