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Nordent Manufacturing Inc

FDA UDI

Class I (US FDA UDI)

by Nordent Manufacturing Inc

Identity

Trade Name
NORDENT MANUFACTURING INC FDA UDI
Generic Name
Margin finishing dental file/rasp, reusable FDA UDI
Device Name
DURALITE MICRO CURVE PADDLE #2 FDA UDI
Model / Reference
REPFI26 FDA UDI
Description
DURALITE MICRO CURVE PADDLE #2 FDA UDI

Identifiers

Primary DI / UDI-DI
00840018635364 FDA UDI
FDA Product Code
EKD FDA UDI
GMDN Term
Margin finishing dental file/rasp, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Margin finishing dental file/rasp, reusable

Nordent Manufacturing Inc by Nordent Manufacturing Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Margin finishing dental file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2c152217-037b-498d-abc3-433ecc8ca136 33 fields · synced May 30, 2026