Europa Thermal Nickel Titanium

TH NITI EUROPA II UPR 017x017 W/STPS

Registry build 21.09.26
43manufacturers in China registered for this device type
20catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Zhejiang (15), Guangdong (9), Jiangsu (6). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DZC
Manufacturer City Province Registered as Device types
Shenzhen Denco Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 52
Shenzhen Rogin Medical Co., Ltd. Shenzhen Guangdong Contract manufacturer 51
Sino Ortho Limited Hangzhou Zhejiang Contract manufacturer 14
Hangzhou Westlake Biomaterial Co., Ltd. Hangzhou Zhejiang Contract manufacturer 13
Zhejiang Eksen Medical Technology Co., Ltd. Huzhou Zhejiang Contract manufacturer 9
Yancheng Denrum Medical Apparatus Co., Ltd. Yancheng Jiangsu Contract manufacturer 5
Heilongjiang Rainbow Technology Co., Ltd. Jiamusi Heilongjiang Contract manufacturer 2
Debo Medical Technology (Shijiazhuang) Co., Ltd. Shijiazhuang Hebei Contract manufacturer 117
Hubei Guarddent Medical Technology Co., Ltd. Wuhan Hubei Manufacturer 60
Shanghai Kangqiao Dental Instruments Factory Shanghai Shanghai Manufacturer 54
Zhejiang Yamei Medical Equipment Technology Co., Ltd. Yang Jiao Lang Zin’An Town Zhejiang Manufacturer 39
Hangzhou Wise Medical Device Co., Ltd. Hangzhou Zhejiang Contract manufacturer 25

Showing 12 of 43. All 43 manufacturers in China registered for Wire, Orthodontic

Record

Regulatory record for Europa Thermal Nickel Titanium
Listed by G & H Wire Company, United States
FDA product code DZC
Device type Wire, Orthodontic
Device class Class 1
Regulation 21 CFR 872.5410
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2025-03-27

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, manufacturing date
Sizes Width 0.016 to 0.025 in; height 0.016 to 0.019 in; outer diameter 0.012 to 0.02 in

Catalogue Numbers

Catalogue numbers for Europa Thermal Nickel Titanium
Catalogue number Size Per pack Status
TEFL014ACB Outer Diameter.014 in 25 In distribution
TEFU1622ACB Width.022 in 25 In distribution
TEFU3717ACB Width.017 in 25 In distribution
TTFU118AD Outer Diameter.018 in 25 In distribution
TEFU1725ACB Height.017 in 25 In distribution
TEFU3725ACB Width.025 in 25 In distribution
TEFL1622ACB Width.022 in 25 In distribution
TEFL3925ACB Height.019 in 25 In distribution
TEFL018ACB Outer Diameter.018 in 25 In distribution
TEFL1725ACB Height.017 in 25 In distribution
TEFL1616ACB Width.016 in 25 In distribution
TEFL3725ACB Width.025 in 25 In distribution
TEFL020ACB Outer Diameter.020 in 25 In distribution
TEFU1825ACB Height.018 in 25 In distribution
TEFL016ACB Outer Diameter.016 in 25 In distribution
TEFU3818ACB Width.018 in 25 In distribution
TEFU3818ADX Height.018 in 10 In distribution
TEFL1825ACB Height.018 in 25 In distribution
TEFL012ACB Outer Diameter.012 in 25 In distribution
TEFL1925ACB Width.025 in 25 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Wire, Orthodontic G & H Wire Company 2,746
Europa G & H Wire Company 2,409
Pg Supply PG Supply, Inc. 1,990
Trueform G & H Wire Company 1,984
G4 Nickel Titanium G & H Wire Company 957
Tanzo American Orthodontics 906
Aditek Aditek DO Brasil S/A 879
G4 Europa Nickel Titanium G & H Wire Company 819
3M™ Unitek™ 3M Unitek 729
Orthodontic wire Dentos, Incorporated 711
Orthoquest Young Innovations Inc. 698
NT3 American Orthodontics 694

Showing 12 of 679. All products under Wire, Orthodontic

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2013-12-13 Class II Employee error Labeling issue: Product labeled as “Upper” may contain “Lower” archwires with a red midline mark. Product labeled ad “Lower” may contain “Upper” archwires with a black midline mark. 9 packages of each lot number. 2014-02-04
2013-12-13 Class II Employee error Labeling issue: Product labeled as “Upper” may contain “Lower” archwires with a red midline mark. Product labeled ad “Lower” may contain “Upper” archwires with a black midline mark. 37 packages 2014-02-04

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer