FDA applicant

Tautona Group, LLC

Menlo Park, CA2 decisions2013–20240 recalls

FDA records 2 decisions for Tautona Group, LLC (Menlo Park, CA) from 2013 to 2024: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and HIF (Insufflator, Laparoscopic). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Tautona Group”.

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

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Tautona Group, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

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

Planning a device like Tautona Group, 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 “Tautona”

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

Tautona Group Research & Development, Co., LLC 1

Tautona Group, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Tautona”