MID-AMERICA SAFETY CORP

FDA Device Registration & Listing · Elk Grove Village, IL, US · Registration 3018382937

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3018382937
FEI Number
3018382937
Entity Name
MID-AMERICA SAFETY CORP
City/State/Country
Elk Grove Village, IL, US
Establishment Address
800 Greenleaf Ave, Elk Grove Village, IL 60007, US
Establishment Type(s)
Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Mid-America Safety Corp (Owner Number: 10081267)
Owner / Operator Contact Address
800 Greenleaf Ave, Elk Grove Village, IL 60007, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MASC MASC Particulate Respirator N95

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FXX Mask, Surgical General, Plastic Surgery Class 2 878.4040 2022-01-04
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2021-03-30

Official Correspondent

Pamela Pan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mid-America Safety Corp
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K201622 Guangdong Kingfa Sci. & Tech.Co., Ltd. Medical surgical mask 2020-11-24
K881618 3M Company ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK 1988-05-09
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018382937. Last updated year: 2026. Please use registration number 3018382937 when referencing this establishment in official correspondence.
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