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ParaPost XP

FDA UDI

Class I (US FDA UDI)

by Coltene/Whaledent Inc.

Identity

Trade Name
ParaPost XP FDA UDI
Generic Name
Root canal post, preformed FDA UDI
Device Name
10 ParaPost XP Plastic Burnout Posts - .055 FDA UDI
Model / Reference
P75155 FDA UDI
Description
10 ParaPost XP Plastic Burnout Posts - .055 FDA UDI

Identifiers

Primary DI / UDI-DI
D661P751551 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

No

FDA UDI

Single Use

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Root canal post, preformed

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

Similar devices

Also classified as Root canal post, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6007ebf4-8ab8-444a-928d-4393aff3b222 33 fields · synced Jun 9, 2026