Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K201483Substantially Equivalent

Impression Material

Zhengzhou Huaer Electro-Optics Technology Co., Ltd., Zhengzhou, CN / Traditional, Substantially Equivalent

K201483 is the FDA 510(k) clearance record for Impression Material, a class II device, cleared for Zhengzhou Huaer Electro Optics Technology Co., Ltd. on under FDA product code ELW (Material, Impression). FDA records list one 510(k) clearance for Zhengzhou Huaer Electro Optics Technology Co., Ltd. As of , FDA records show no recalls naming K201483.

Clearance record

Decision date
Received
(126 days to decision)
Product code
ELW Material, Impression
Regulation
21 CFR 872.3660
Device class
Class II
Review panel
Dental
Applicant
Zhengzhou Huaer Electro Optics Technology Co., Ltd. Floor 1, B Of Bldg. 18, National University Science Park, Zhengzhou, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ELW

Trailing 12 months
3 clearances under product code ELW in the twelve months to October 2026, September 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code ELW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20262
October 20260