Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012094493

FEI Number

3012094493

Entity Name

JMS MANUFACTURING, INC.

City/State/Country

Omaha, NE, US

Establishment Address

8805 Vernon Ave, Omaha, NE 68134, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

JMS Manufacturing, Inc. (Owner Number: 10050231)

Owner / Operator Contact Address

8805 Vernon Ave., Omaha, NE 68134, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Soft-Prop C-Prop Mouth Prop E-Prop Bite DX

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BRW	Protector, Dental	Anesthesiology	Class 1	868.5820	2015-10-23
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2017-02-01

Official Correspondent

Steven Kempkes

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JMS Manufacturing, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012094493. Last updated year: 2026. Please use registration number 3012094493 when referencing this establishment in official correspondence.