FDA applicant

Convergent Dental, Inc.

Austin, TX4 decisions2013–20222 recalls

FDA records 4 decisions for Convergent Dental, Inc. (Austin, TX) from 2013 to 2022: 4 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and NVK (Laser, Dental, Soft Tissue). Its devices cite 9 predicates, 4 of them its own earlier devices. 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Convergent Dental, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2013high 2 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

1in 2023

2013high 1 (2013) · low 0 (2014)2026

Class I Class II/III not classified

FIG. 1 — Convergent Dental, Inc. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Convergent Dental, Inc.’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 “Convergent”

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

Convergent Laser Technologies 2 Convergent Imaging Solutions 2 Convergent Life Sciences, Inc. 1

Convergent Dental, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Convergent”