ET Angled Abutment

30 catalogue numbers from ETAA4020MBC, listed by Hiossen Inc., United States, under Abutment, Implant, Dental, Endosseous. 15 manufacturers in China are registered for this product code.

Registry build 21.09.26
15manufacturers in China registered for this device type
30catalogue numbers in this listing
9510(k) clearances naming this product code
6recalls on this code

Who Else Makes It

Concentrated in Guangdong (11), Jiangsu (2), Shanghai (1). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code NHA
Manufacturer City Province Registered as Device types
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Modern Dental Laboratory (DG) Co., Ltd. Dongguan Guangdong Contract manufacturer 15
Exceldent Dental Technology Development Co., Ltd. Zhuhai Guangdong Contract manufacturer 12
DTS Digital Dental LAB Shenzhen Guangdong Contract manufacturer 11
KTJ Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Shimmer Computerized Dental Technology Co., Ltd. Zhuhai Guangdong Contract manufacturer 10
Zhuhai Crystal Dental Technology Co., Ltd. Zhuhai Guangdong Contract manufacturer 9
NEW Perfect Dental LAB Shenzhen Guangdong Contract manufacturer 8
Shenzhen Jiahong Dental Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 7
Jiangsu Trausim Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
Chengdu Besmile Medical Technology Co., Ltd. Chengdu Sichuan Manufacturer 14
CBD Dental LAB, Inc Shenzhen Guangdong Manufacturer 11

Showing 12 of 15. All 15 manufacturers in China registered for Abutment, Implant, Dental, Endosseous

Record

Regulatory record for ET Angled Abutment
Listed by Hiossen Inc., United States
FDA product code NHA
Device type Abutment, Implant, Dental, Endosseous
Device class Class 2
Regulation 21 CFR 872.3630
Establishment Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K222636
Record published 2024-07-05
Record revised 2025-07-02 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for ET Angled Abutment
Catalogue number Size Status
ETAA4020MBC In distribution
ETAA5040BC In distribution
ETAA4520AC In distribution
ETAA4540MAC In distribution
ETAA4520MBC In distribution
ETAA6040BC In distribution
ETAA4540MBC In distribution
ETAA4540AC In distribution
ETAA4520BC In distribution
ETAA5020BC In distribution
ETAA6040AC In distribution
ETAA4540MNC In distribution
ETAA6020AC In distribution
ETAA4540NC In distribution
ETAA6040NC In distribution
ETAA4040MNC In distribution
ETAA4040MAC In distribution
ETAA5040AC In distribution
ETAA6020BC In distribution
ETAA4520MNC In distribution
ETAA5040NC In distribution
ETAA5020AC In distribution
ETAA4040MBC In distribution
ETAA5020NCWH In distribution
ETAA6020NC In distribution
ETAA4020MACWH In distribution
ETAA4020MNC In distribution
ETAA4520NC In distribution
ETAA4540BC In distribution
ETAA4520MAC In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
MEDENTiKA Medentika GmbH 2,553
LW Vis Abutment Ossvis Co., Ltd. 2,520
Dess dental smart solutions Terrats Medical SL 1,715
Locator Zest Anchors, LLC 1,643
NobelProcera® Nobel Biocare AB 1,526
Azure Terrats Medical SL 1,360
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 1,308
LW Vis Abutment SET Ossvis Co., Ltd. 1,260
Abutment, Implant, Dental, Endosseous Southern Implants (PTY) Ltd 1,240
Healing Abutment Megagen Implant Co., Ltd. 1,218
Chaorum Implant System Medimecca Co Ltd 1,084
OT Equator Rhein 83 SRL 1,051

Showing 12 of 6,204. All products under Abutment, Implant, Dental, Endosseous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253372 2026-05-14
K251427 2026-01-29
K241003 2025-01-08
K233389 2024-05-29
K222636 2023-04-28
K170421 2018-01-11
K162390 2017-01-30
K132067 2013-12-20
K123627 2013-06-28

Recalls

6 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
2025-01-27 Class II Under Investigation by firm Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product 48
2025-01-27 Class II Under Investigation by firm Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product 19 units
2025-01-27 Class II Under Investigation by firm Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product 16 units
2025-01-27 Class II Under Investigation by firm Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product 19 units
2025-01-27 Class II Under Investigation by firm Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product 119 units
2025-01-27 Class II Under Investigation by firm Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product 19

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