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ZenSeal

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
ZenSeal FDA UDI
Generic Name
Hygroscopic dental cement FDA UDI
Device Name
Bio Ceramic Root Canal Sealer Syringe and (2x10Pk) Disposable Tips FDA UDI
Model / Reference
825-9501 FDA UDI
Description
Bio Ceramic Root Canal Sealer Syringe and (2x10Pk) Disposable Tips FDA UDI

Identifiers

Primary DI / UDI-DI
00195062076381 FDA UDI
FDA Product Code
KIF FDA UDI
GMDN Term
Hygroscopic dental cement FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Dimensions & Sizes

Size
Weight — 2 Gram FDA UDI

Category: Hygroscopic dental cement

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

Similar devices

Also classified as Hygroscopic dental cement.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI c0a37a93-7746-46c6-acfd-5d4940f990f5 36 fields · synced Jun 8, 2026