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Kör

FDA UDI

Class II (US FDA UDI)

by Evolve Dental Technologies, Inc.

Identity

Trade Name
KöR FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Vinyl Polysiloxane Putty - Regular set impression material. FDA UDI
Model / Reference
KöR Putty - Regular Set FDA UDI
Description
Vinyl Polysiloxane Putty - Regular set impression material. FDA UDI

Identifiers

Catalog Number
10-1014 FDA UDI
Primary DI / UDI-DI
00850362007014 FDA UDI
510(k) Number
K821221 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

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: Silicone dental impression material

Kör by Evolve Dental Technologies, Inc. — 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 fa2850db-98e7-4447-810f-da67d782ce50 37 fields · synced Jun 6, 2026