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Biocryl Ice 1# Polymer

FDA UDI

Class II (US FDA UDI)

by Great Lakes Dental Technologies

Identity

Trade Name
BIOCRYL ICE 1# POLYMER FDA UDI
Generic Name
Dental prosthesis restorative material, unfilled resin FDA UDI
Model / Reference
047-003 FDA UDI

Identifiers

Primary DI / UDI-DI
D7750470030 FDA UDI
510(k) Number
K112397 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental prosthesis restorative material, unfilled resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Dental prosthesis restorative material, unfilled resin

Biocryl Ice 1# Polymer by Great Lakes Dental Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis restorative material, unfilled resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9327eb3d-56e5-460d-a230-205870229932 34 fields · synced Jun 6, 2026