FDA applicant

Faxitron Bioptics, LLC

Tucson, AZ5 decisions2012–20190 recalls

FDA records 5 decisions for Faxitron Bioptics, LLC (Tucson, AZ) from 2012 to 2019: 5 510(k) clearances. All are in product code MWP (Cabinet, X-Ray System). Its devices cite 11 predicates, 5 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, radiology panel, where it files most

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

FDA decisions per year

1in 2019

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

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

Planning a device like Faxitron Bioptics, 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 “Faxitron”

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

Faxitron X-Ray Corp. 2

Faxitron Bioptics, 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 “Faxitron”