TWIN CITY EDM AND MFG INC

FDA Device Registration & Listing · Fridley, MN, US · Registration 3007841013

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
3007841013
FEI Number
3007841013
Entity Name
TWIN CITY EDM AND MFG INC
City/State/Country
Fridley, MN, US
Establishment Address
7940 Ranchers Rd NE, Fridley, MN 55432, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
TWIN CITY EDM AND MFG INC (Owner Number: 10044560)
Owner / Operator Contact Address
7940 Ranchers Road NE, Fridley, MN 55432, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Screwdriver CORE Shoulder System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HXX Screwdriver Orthopedic Class 1 888.4540 2023-10-25
QHE Shoulder Arthroplasty Implantation System Orthopedic Class 2 888.3660 2025-06-18
GFC Driver, Surgical, Pin General, Plastic Surgery Class 1 878.4820 2023-10-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TWIN CITY EDM AND MFG INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007841013. Last updated year: 2026. Please use registration number 3007841013 when referencing this establishment in official correspondence.
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