510(k) Report

FDA applicant

Implant Protesis Dental 2004, S.L.

Premià De Dalt (Barcelona), ES6 decisions2022–20260 recalls

FDA records 6 decisions for Implant Protesis Dental 2004, S.L. (Premià De Dalt (Barcelona), ES) from 2022 to 2026: 6 510(k) clearances. All are in product code NHA (Abutment, Implant, Dental, Endosseous). Since 2016 its 510(k)s took a median of 99 days from receipt to decision, against 153 for FDA’s reviews in the same codes and years. Its devices cite 6 predicates, 4 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 Protesis Dental 2004, S.L.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2022: 12023: 12024: 22025: 12026 (partial year): 1
2022high 2 (2024) · low 1 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Implant Protesis Dental 2004, S.L. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Implant Protesis Dental 2004, S.L.’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.