← Back to catalogue

Zinc Phosphate

FDA UDI

Class II (US FDA UDI)

by Shofu Dental Corp.

Identity

Trade Name
Zinc Phosphate FDA UDI
Generic Name
Zinc phosphate dental cement FDA UDI
Device Name
HY-BOND ZINC POWDER FDA UDI
Model / Reference
1171 FDA UDI
Description
HY-BOND ZINC POWDER FDA UDI

Identifiers

Catalog Number
1171 FDA UDI
Primary DI / UDI-DI
E23511710 FDA UDI
510(k) Number
K810765 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Zinc phosphate dental cement FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Zinc phosphate dental cement

Zinc Phosphate by Shofu Dental Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Zinc phosphate dental cement.

Cleared under the same submission

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

Manufacturer
Shofu Dental Corp.

Sources (1)

  • FDA UDI 9153aa83-7222-4df9-b02d-31df75485970 36 fields · synced Jun 6, 2026