510(k) Report

FDA applicant

Medical Modeling, Inc.

Washington, DC2 decisions2012–20141 recall

FDA records 2 decisions for Medical Modeling, Inc. (Washington, DC) from 2012 to 2014: 2 510(k) clearances. All are in product code DZJ (Driver, Wire, And Bone Drill, Manual). Its devices cite 5 predicates, 1 of them its own earlier devices. 1 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 Medical Modeling, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2012: 12014: 1
2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

1in 2022

2022: 1
2012high 1 (2022) · low 0 (2012)2026

Class I Class II/III not classified

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

Planning a device like Medical Modeling, 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