STURGIS MOLDED PRODUCTS COMPANY

FDA Device Registration & Listing · Sturgis, MI, US · Registration 3000170790

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
3000170790
FEI Number
3000170790
Entity Name
STURGIS MOLDED PRODUCTS COMPANY
City/State/Country
Sturgis, MI, US
Establishment Address
1950 Clark Rd, Sturgis, MI 49091, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Sturgis Molded Products Company (Owner Number: 10053177)
Owner / Operator Contact Address
1950 Clark Street, Sturgis, MI 49091, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dose Cup

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2016-11-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sturgis Molded Products Company
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 3000170790. Last updated year: 2026. Please use registration number 3000170790 when referencing this establishment in official correspondence.
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