Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027386225

FEI Number

3027386225

Entity Name

ENTERRA MEDICAL, INC.

City/State/Country

Saint Louis Park, MN, US

Establishment Address

5353 Wayzata Blvd., Suite 400, Saint Louis Park, MN 55416, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Enterra Medical, Inc. (Owner Number: 10088127)

Owner / Operator Contact Address

5353 Wayzata Blvd., Suite 400, Saint Louis Park, MN 55416, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

H990014

All Registered Proprietary Names

Enterra II ReliaStim

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LNQ	Intestinal Stimulator	Unknown	Class f	N/A	2023-05-30

Official Correspondent

Bernard Bosley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Enterra Medical, 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 3027386225. Last updated year: 2026. Please use registration number 3027386225 when referencing this establishment in official correspondence.