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Candid Refinement Impression Kit

FDA UDI

Class II (US FDA UDI)

by Candid Care Co.

Identity

Trade Name
Candid Refinement Impression Kit FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Refinement Impression Kit (Medium Trays) Kett Putty Digital FDA UDI
Model / Reference
ITISK00001 FDA UDI
Description
Refinement Impression Kit (Medium Trays) Kett Putty Digital FDA UDI

Identifiers

Primary DI / UDI-DI
00850004223987 FDA UDI
510(k) Number
K082560 FDA UDI
FDA Product Code
ELW FDA UDI
EHY FDA UDI
EIG FDA UDI
GMDN Term
Silicone dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
872.6880 FDA UDI
872.4565 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Silicone dental impression material

Candid Refinement Impression Kit by Candid Care Co. — 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

Manufacturer
Candid Care Co.

Sources (1)

  • FDA UDI 5cb0dcfe-5ac3-428c-8728-a98073136078 35 fields · synced May 30, 2026