ANNEX MEDICAL, INC.

FDA Device Registration & Listing · Minnetonka, MN, US · Registration 2183873

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
2183873
FEI Number
2183873
Entity Name
ANNEX MEDICAL, INC.
City/State/Country
Minnetonka, MN, US
Establishment Address
6018 BLUE CIRCLE DR., Minnetonka, MN 55343, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ANNEX MEDICAL, INC. (Owner Number: 2183873)
Owner / Operator Contact Address
6018 BLUE CIRCLE DR., --, Minnetonka, MN 55343, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

6-Wire Halo Nitinol Tipless Stone Basket Halo Trinity Nitinol Tipless Stone Basket Hercules Paired Helical Stone Basket Halo Nitinol Tipless Stone Basket Vantage Nitinol Tipless Stone Basket Apex Nitinol Flat Wire Stone Basket

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FFL Dislodger, Stone, Basket, Ureteral, Metal Gastroenterology, Urology Class 2 876.4680 1992-11-27
FDX Endoscopic Cytology Brush Gastroenterology, Urology Class 2 876.1500 2008-04-23

Official Correspondent

STUART LIND

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2023 Hobbs Medical, Inc. 2
Hobbs Medical Cytology Brush Catalog Number: 4204
Z-0014-2023 Hobbs Medical, Inc. 2
Hobbs Medical Cytology Brush Catalog Number: 4206

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183873. Last updated year: 2026. Please use registration number 2183873 when referencing this establishment in official correspondence.
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