Phoenix Orthodontics Inc

FDA Device Registration & Listing · Marietta, GA, US · Registration 3009491780

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
3009491780
FEI Number
3009491780
Entity Name
Phoenix Orthodontics Inc
City/State/Country
Marietta, GA, US
Establishment Address
3750 Palladian Village Drive, Building 400 Suite 410, Marietta, GA 30066, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Phoenix Orthodontics Inc (Owner Number: 10040049)
Owner / Operator Contact Address
1565 Sandpoint Drive NE, Roswell, GA 30075, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Endura High Performance Chain Spectrum Elastomerics Phoenix “M” Series Molar Bands Phoenix Symmetry iP Phoenix “Original” Series Molar Bands Phoenix Stainless Steel Wires Phoenix Nickel Titanium Wires Phoenix Stainless Kobayashi Tie Hooks Phoenix Optimal Phoenix Convertible Buccal Tubes Phoenix Wire Forming Instruments Phoenix Wire Cutters

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ECI Band, Elastic, Orthodontic Dental Class 1 872.5410 2012-03-04
ECM Band, Preformed, Orthodontic Dental Class 1 872.5410 2023-09-22
DZD Tube, Orthodontic Dental Class 1 872.5410 2023-09-22
DZN Instruments, Dental Hand Dental Class 1 872.4565 2023-09-22

Official Correspondent

John Burhans

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Phoenix Orthodontics 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 3009491780. Last updated year: 2026. Please use registration number 3009491780 when referencing this establishment in official correspondence.
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