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Ultra Dispersed Phase

FDA UDI

Class II (US FDA UDI)

by DMG America LLC

Identity

Trade Name
Ultra Dispersed Phase FDA UDI
Generic Name
Dental amalgam FDA UDI
Device Name
Ultra Dispersed Phase Dental Amalgam Alloy 1 Spill Regular Set 500 jar FDA UDI
Model / Reference
55068 FDA UDI
Description
Ultra Dispersed Phase Dental Amalgam Alloy 1 Spill Regular Set 500 jar FDA UDI

Identifiers

Catalog Number
099-55068 FDA UDI
Primary DI / UDI-DI
D033099550681 FDA UDI
510(k) Number
K820617 FDA UDI
FDA Product Code
EJJ FDA UDI
GMDN Term
Dental amalgam FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3070 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 400 Milligram FDA UDI

Category: Dental amalgam

Ultra Dispersed Phase by DMG America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental amalgam.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DMG America LLC

Sources (1)

  • FDA UDI 14cd59a5-07fc-44f1-88ea-e171b23bd95b 38 fields · synced Jun 8, 2026