FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Denture Base Resin DT20

K Number: K250946 · Decision Mar 31, 2025
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
5
Review Days
3

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Denture Base Resin DT20
K Number
K250946
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hangzhou SHINING3D Dental Technology Co., Ltd.
Date Received
March 28, 2025
Decision Date
March 31, 2025
Product Code
EBI
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EBI Resin, Denture, Relining, Repairing, Rebasing

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EBI), ordered by most recent decision date.

View all

Other Clearances by Hangzhou SHINING3D Dental Technology Co., Ltd.

K Number Device Name
K261356 Dura-Crown
K261261 Dura-Arch
K260170 LumiCera
K253053 Dura-Crown (CB21-A1/CB21-A2/CB21-A3/CB21-B1)