TAURUS ENGINEERING AND MANUFACTURING, INC.

FDA Device Registration & Listing · Saint Paul, MN, US · Registration 3010236732

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
3010236732
FEI Number
3010236732
Entity Name
TAURUS ENGINEERING AND MANUFACTURING, INC.
City/State/Country
Saint Paul, MN, US
Establishment Address
1375 WILLOW LAKE BLVD # 101, Saint Paul, MN 55110, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Taurus Engineering and Manufacturing, Inc. (Owner Number: 10045742)
Owner / Operator Contact Address
1375 Willow Lake Blvd, Suite 101, Vadnais Heights, MN 55110, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MULTI ADJUSTABLE FACE MASK CorrectClips

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EIG Retractor, All Types Dental Class 1 872.4565 2018-09-19
EIL Gauge, Depth, Instrument, Dental Dental Class 1 872.4565 2017-07-27
DZB Headgear, Extraoral, Orthodontic Dental Class 2 872.5500 2013-12-23
ECI Band, Elastic, Orthodontic Dental Class 1 872.5410 2017-07-27
ECS Pusher, Band, Orthodontic Dental Class 1 872.4565 2017-07-27
MJI Specimen/Tissue, Identification Orientation Pathology Class 1 864.3010 2021-12-21

Official Correspondent

John Philipsen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Taurus Engineering and Manufacturing, 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-0012-2012 Biomet Microfixation, Inc. 1
Biomet Microfixation outer packaging labeled in part:"REF: SP-2411***RUBBER BAND, LATEX FREE SMALL, HEAVY, 300/PACKAGE 4MM, (3/16" INNER DIAMETER) NON LATEX ELASTICS LOT 307850***DISTRIBUTED BY: BIOMET MICROFIXATION 1520 Tradeport Drive, Jacksonville, FL 32218 USA www.biometmicrofixation.com***." Inner Vendor/Manufacturer Label labeled in part:"H4 Elastics 4mm (3/16") Heavy 4 oz. REF 11-102-04***Manufactured for DENTSPLY GAC INTERNATIONAL DENTSPLY INTERNATIONAL, INC. Phone 631-419-1700 Fax 631-419-1599 355 Knickerbocker Avenue Bohemia NY 11716 USA***MediMark Europe BP2332 F-38033 Grenoble Cedex 2. France***LOT 82936-32 QTY:100 pk use by 2012-07 Made in USA ISSUED DATE 2009-04 GN***" Elastic bands used as elastomeric ties for ligation that facilitate treatment of fracture of the mandible and maxilla. They are commonly used with braces or arch bar wire.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010236732. Last updated year: 2026. Please use registration number 3010236732 when referencing this establishment in official correspondence.
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