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Correct Plus

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Correct Plus FDA UDI
Generic Name
Silicone dental impression material FDA UDI
Device Name
Mighty Mix; Hydrophilic Vinyl Polysiloxane Impression Material; 5:1 Cartridge System; Auto-Mix Putty FDA UDI
Model / Reference
Q34MB FDA UDI
Description
Mighty Mix; Hydrophilic Vinyl Polysiloxane Impression Material; 5:1 Cartridge System; Auto-Mix Putty FDA UDI

Identifiers

Primary DI / UDI-DI
10814978022998 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

Dimensions & Sizes

Size
Total Volume — 760 Milliliter FDA UDI

Category: Silicone dental impression material

Correct Plus by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI e4cb023d-8537-47cd-a456-648b5bd456c0 36 fields · synced Jun 8, 2026