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Obtura Spartan

FDA UDI

Class I (US FDA UDI)

by Young Innovations, Inc.

Identity

Trade Name
Obtura Spartan FDA UDI
Generic Name
Endodontic plugger FDA UDI
Device Name
Obtura Max Plunger Shaft Assy. FDA UDI
Model / Reference
823-812 FDA UDI
Description
Obtura Max Plunger Shaft Assy. FDA UDI

Identifiers

Catalog Number
823-812 FDA UDI
Primary DI / UDI-DI
00843471100288 FDA UDI
510(k) Number
K042828 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Endodontic plugger FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endodontic plugger

Obtura Spartan by Young Innovations, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic plugger.

Cleared under the same submission

K042828 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8a6a9d61-b518-4202-9ea1-6a250b33d7f3 36 fields · synced Jun 8, 2026