FDA applicant

Sterngold Dental, LLC

Attleboro, MA12 decisions2012–20170 recalls

FDA records 12 decisions for Sterngold Dental, LLC (Attleboro, MA) from 2012 to 2017: 12 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and NHA (Abutment, Implant, Dental, Endosseous). Its devices cite 25 predicates, 7 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 Sterngold Dental, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2012high 4 (2015) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Sterngold Dental, LLC by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sterngold Dental, LLC’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 “Sterngold”

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

Sterngold/Implamed 16 Sterngold 12

Sterngold Dental, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Sterngold”