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Chemoment

FDA UDI

Class II (US FDA UDI)

by Chemoment Materials Co., Ltd.

Identity

Trade Name
Chemoment FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Model / Reference
2 FDA UDI

Identifiers

Primary DI / UDI-DI
06976009582226 FDA UDI
510(k) Number
K221668 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Silicone dental impression material

Chemoment by Chemoment Materials Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

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 e0e406a3-3098-491b-ad93-50c662c5680e 33 fields · synced Jun 8, 2026