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Absolute Dentin™

FDA UDI

Class II (US FDA UDI)

by Parkell, Inc.

Identity

Trade Name
Absolute Dentin™ FDA UDI
Generic Name
Dental material injection cannula, single-use FDA UDI
Device Name
Yellow Intraoral Tip for Use on S302 Mixing Tip (Pkg. of 50 pcs.) FDA UDI
Model / Reference
S303 FDA UDI
Description
Yellow Intraoral Tip for Use on S302 Mixing Tip (Pkg. of 50 pcs.) FDA UDI

Identifiers

Catalog Number
S303 FDA UDI
Primary DI / UDI-DI
10810000526878 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Dental material injection cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

No

FDA UDI

Category: Dental material injection cannula, single-use

Absolute Dentin™ by Parkell, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material injection cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Parkell, Inc.

Sources (1)

  • FDA UDI 354842eb-701f-4455-8721-b077c84e565c 35 fields · synced May 31, 2026