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ParaPost XP P75155

by Coltene/Whaledent Inc.

ParaPost XP P75155 is a Class I device made by Coltene/Whaledent Inc., listed in FDA GUDID since 11 Feb 2019 (UDI-DI D661P751551), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD661P751551 UDI-DI Date11 Feb 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
ParaPost XP
Generic name
Root canal post, preformed
Model / reference
P75155
Primary DI / UDI-DI
D661P751551
FDA product code
ELR
GMDN term
Root canal post, preformed
Device class
Class I
Regulation number
872.3810
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Root canal post, preformed

Similar devices in this category

Other devices filed under Root canal post, preformed.

Other devices from Coltene/Whaledent Inc.

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Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)