← Back to catalogue

Cast Frame & Partial Denture Pure Titanium

FDA UDI

Class N (US FDA UDI)

by Beijing Yingguan Dental Technology Co., Ltd.

Identity

Trade Name
Cast Frame & Partial Denture Pure Titanium FDA UDI
Generic Name
Partial denture FDA UDI
Model / Reference
/ FDA UDI

Identifiers

Primary DI / UDI-DI
06975031821013 FDA UDI
FDA Product Code
NSK FDA UDI
GMDN Term
Partial denture FDA UDI

Classification

Device Class
N FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Partial denture

Cast Frame & Partial Denture Pure Titanium by Beijing Yingguan Dental Technology Co., Ltd. — Class N — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Partial denture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 6a79fe4e-7bef-46e2-a90e-d0c61615e092 32 fields · synced Jun 1, 2026