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Essentials

FDA UDI

Class II (US FDA UDI)

by Mdc Dental

Identity

Trade Name
ESSENTIALS FDA UDI
Generic Name
Alginate dental impression material FDA UDI
Device Name
ALGINATE ESSENTIALS ALL PURPOSE TYPE I 1LB FDA UDI
Model / Reference
ESSENTIALS FDA UDI
Description
ALGINATE ESSENTIALS ALL PURPOSE TYPE I 1LB FDA UDI

Identifiers

Primary DI / UDI-DI
07506338321631 FDA UDI
510(k) Number
K011785 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Alginate 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Alginate dental impression material

Essentials by Mdc Dental — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alginate 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
Mdc Dental

Sources (1)

  • FDA UDI 9a57779c-044d-4999-a580-3f29bffedfa7 35 fields · synced Jun 8, 2026