ParaPost

FDA UDI

Class I (US FDA UDI)

by Coltene/Whaledent Inc.

Identity

Trade Name: ParaPost FDA UDI
Generic Name: Root canal post, preformed FDA UDI
Device Name: PARAPOST FIBERLUX SIZE 3 FDA UDI
Model / Reference: PF1713C FDA UDI
Description: PARAPOST FIBERLUX SIZE 3 FDA UDI

Identifiers

Primary DI / UDI-DI: D661PF1713C1 FDA UDI
FDA Product Code: ELR FDA UDI
GMDN Term: Root canal post, preformed FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3810 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Root canal post, preformed

ParaPost by Coltene/Whaledent Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Coltene/Whaledent Inc.

Sources (1)

FDA UDI 0b924cc1-a8ca-4463-a6e2-0539dcb6a48c 34 fields · synced Jun 9, 2026