AtriCure - Minneapolis

FDA Device Registration & Listing · Minnetonka, MN, US · Registration 3011788769

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
3011788769
FEI Number
3011788769
Entity Name
AtriCure - Minneapolis
City/State/Country
Minnetonka, MN, US
Establishment Address
130 Cheshire Ln Ste 250, Minnetonka, MN 55305, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ATRICURE, INC. (Owner Number: 9045049)
Owner / Operator Contact Address
7555 Innovation Way, --, Mason, OH 45040, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

AtriCure cryoICE cryoFORM cryoablation probe (CRYOF) CRYO3 - AtriCure cryoICE cryo-ablation probe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEH Unit, Cryosurgical, Accessories General, Plastic Surgery Class 2 878.4350 2016-03-25
GEH Unit, Cryosurgical, Accessories General, Plastic Surgery Class 2 878.4350 2015-04-03

Official Correspondent

Janet Hillard

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ATRICURE, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3020954746 AtriCure, Inc. Pleasanton, CA, US
3011706110 ATRICURE, INC. Mason, OH, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K190651 Erbe Elektromedizin GmbH ERBECRYO 2 Cryosurgical Unit; ERBECRYO 2 1-pedal footswitch, Extension cable f. ERBECRYO 2 footswitch; Flexible Cryoprobe; ERBECRYO 2 Cart, VIO-Cart, Wire basket; Connecting hoses, switching valves, adapter 2020-01-07
K760953 Spembly Medical , Ltd. DEEP FREEZE SYSTEM (DFS-30) 1976-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011788769. Last updated year: 2026. Please use registration number 3011788769 when referencing this establishment in official correspondence.
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