MID-AMERICA SAFETY CORP

Contract manufacturer · Elk Grove Village, IL

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

FDA registration

3018382937 (openFDA record; or search FDA's registration database)

FEI number

3018382937

Registered for

FDA registration year 2026

Establishment types

Manufacturer; Contract manufacturer; Repackager or relabeler

Owner or operator

Mid-America Safety Corp (FDA owner/operator no. 10081267)

Registered address

800 Greenleaf Ave, Elk Grove Village, IL 60007

Contract listings

1 device listings, 1 product codes, first listed Mar 30, 2021

Certification

Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.