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Tytin FC

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Tytin FC FDA UDI
Generic Name
Dental amalgam alloy FDA UDI
Device Name
Self-Activating Capsule - Fast Set - Firm Packing Dental Amalgam - Triple Spill FDA UDI
Model / Reference
29996 FDA UDI
Description
Self-Activating Capsule - Fast Set - Firm Packing Dental Amalgam - Triple Spill FDA UDI

Identifiers

Primary DI / UDI-DI
10841396117845 FDA UDI
FDA Product Code
EJJ FDA UDI
GMDN Term
Dental amalgam alloy 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 — 800 Milligram FDA UDI

Category: Dental amalgam alloy

Tytin FC by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental amalgam alloy.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI d8a27ab2-7733-4d47-a74e-b72dc7e7e337 36 fields · synced Jun 8, 2026