Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030495169

FEI Number

3030495169

Entity Name

Ekcomed, Inc.

City/State/Country

Waverly, MN, US

Establishment Address

318 Pacific Avenue, Waverly, MN 55390, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Ekcomed, Inc. (Owner Number: 10090114)

Owner / Operator Contact Address

4253 Queens Way, Minnetonka, MN 55345, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Support, Patient Position Forceps

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2024-02-16
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2024-02-16

Official Correspondent

Richard Barrett

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ekcomed, 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
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030495169. Last updated year: 2026. Please use registration number 3030495169 when referencing this establishment in official correspondence.