FDA applicant

Mcghan Medical Corp.

Santa Barbara, CA14 decisions1978–19875 recalls

FDA records 14 decisions for Mcghan Medical Corp. (Santa Barbara, CA) from 1978 to 1987: 14 510(k) clearances. Most are in product codes LCJ (Tissue Expander And Accessories) and GEY (Motor, Surgical Instrument, Ac-Powered). 5 recalls are linked to its devices, 3 Class I.

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

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Mcghan Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mcghan Medical Corp. since 2007.

Recalls per year

1in 2023

2007high 3 (2019) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Mcghan Medical Corp.’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 “Mcghan”

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

Mcghan Instrumed Corp. 1

Mcghan Medical Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Mcghan”