Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2110701

FEI Number

2110701

Entity Name

ULMER PHARMACAL CO.

City/State/Country

PARK RAPIDS, MN, US

Establishment Address

1614 INDUSTRIAL AVE W, PARK RAPIDS, MN 56470, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ULMER PHARMACAL CO. (Owner Number: 9002102)

Owner / Operator Contact Address

1614 Industry Avenie, --, Park Rapids, MN 56470, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMJ	Lubricant, Patient	General Hospital	Class 1	880.6375	2014-02-06

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ULMER PHARMACAL CO.

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
K820587	Abco Dealers, Inc.	WET PACK LINE OF PRODUCTS	1982-03-26

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1222928	Primo Medical Group, INC	STOUGHTON, MA, US
2212018	PARKER LABORATORIES, INC.	FAIRFIELD, NJ, US
1043214	DEROYAL INDUSTRIES, INC.	POWELL, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2110701. Last updated year: 2026. Please use registration number 2110701 when referencing this establishment in official correspondence.