FDA applicant

Implants Microdent System S.L

Santa Eulalia De Roncana, ES1 decision2016–20160 recalls

FDA records 1 decision for Implants Microdent System S.L (Santa Eulalia De Roncana, ES) in 2016: 1 510(k) clearance. All are in product code DZE (Implant, Endosseous, Root-Form). Its devices cite 1 predicate, 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 Implants Microdent System S.L’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Implants Microdent System S.L by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Implants Microdent System S.L’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 “Implants”

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

Implants International, Ltd. 2 Implants Intl., Ltd. 1 Implants Diffusion International 1

Implants Microdent System S.L

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Implants”