510(k) Report

FDA applicant

Med-Tec, Inc. D/B/A Civco Medical Solutions

Orange City, IA2 decisions2012–20132 recalls

FDA records 2 decisions for Med-Tec, Inc. D/B/A Civco Medical Solutions (Orange City, IA) from 2012 to 2013: 2 510(k) clearances. All are in product code JAI (Couch, Radiation Therapy, Powered). Its devices cite 1 predicate, 0 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, radiology panel, where it files most

How often FDA has decided Med-Tec, Inc. D/B/A Civco Medical Solutions’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2012: 12013: 1
2012high 1 (2012) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

1in 2017

2016: 12017: 1
2012high 1 (2016) · low 0 (2012)2026

Class I Class II/III not classified

FIG. 1 — Med-Tec, Inc. D/B/A Civco Medical Solutions by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Med-Tec, Inc. D/B/A Civco Medical…’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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