FDA applicant

Lares Research, Inc.

Chico, CA10 decisions1991–20220 recalls

FDA records 10 decisions for Lares Research, Inc. (Chico, CA) from 1991 to 2022: 10 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and GEX (Powered Laser Surgical Instrument). Its devices cite 9 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Lares Research”.

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 Lares Research, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2022

2007high 2 (2022) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lares Research, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Lares Research, Inc.’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 “Lares”

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

Lares Manufacturing Co., Inc. 6

Lares Research, Inc.

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 “Lares”