MG Development America Inc.

FDA Device Registration & Listing · Pittsburgh, PA, US · Registration 3010602043

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
3010602043
FEI Number
3010602043
Entity Name
MG Development America Inc.
City/State/Country
Pittsburgh, PA, US
Establishment Address
187 36th St, Pittsburgh, PA 15201, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MG Development America Inc. (Owner Number: 10045525)
Owner / Operator Contact Address
187 36th St., Pittsburgh, PA 15201, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Drying Capsule Gel Care For Hearing Aids Unit, Drying PerfectDry Desinfecting Wipes For Hearing Aids Drying Kit Cleansing Stick For Hearing Aids Cleansing Spray, Wipes And Tablets For Hearing Aids PerfectDry Lux Drying Cup Vanity For Hearing Aids Drying Air Ball & Drying Small Cloth For Hearing Aids PerfectDome PerfectDry QR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2013-11-26
KEM Agent, Clearing Pathology Class 1 864.4010 2020-01-15
ESD Hearing Aid, Air-Conduction, Prescription Ear, Nose, Throat Class 1 874.3300 2020-01-15

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MG Development America Inc.
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
K892457 Telstar Electronics, Inc. TELSTAR MODEL 1/3 ITE HEARING AID 1989-06-06
K760996 Unitron Industries, Inc. HEARING AID (MODEL 695D, 905 & 960P) 1976-11-16
K840825 Maico Hearing Instruments, Inc. SERIES MR IN-THE-EAR CUSTOM HEARING AID 1984-03-30
K946253 Maico Hearing Instruments, Inc. MAICO IN-THE-EAR MODEL RD 201 1995-01-30
K863975 Gn Danavox, Inc. CUSTOM IN-THE-EAR 1986-11-07

Similar Registrations

Registration Number Establishment Name Location
3014420447 DIVERSEY, INC. Fort Mill, SC, US
3012117386 TOMI ENVIRONMENTAL SOLUTIONS, INC. Frederick, MD, US
3007031049 MINIPAC PRODUCTS LTD Kadima-Zoran Central, IL
3008697511 Geann Industrial Co Ltd Lukang Town Changhua, TW
1526481 KLEEN TEST PRODUCTS CORPORATION Strasburg, OH, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010602043. Last updated year: 2026. Please use registration number 3010602043 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.