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Frc Postec Plus 603541AN

by Ivoclar Vivadent Aktiengesellschaft

Frc Postec Plus 603541AN is a Class I device made by Ivoclar Vivadent Aktiengesellschaft, listed in FDA GUDID since 16 Nov 2018 (UDI-DI DVIV603541AN1), 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 NumberDVIV603541AN1 UDI-DI Date16 Nov 2018ListedStatusListed 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  • Withdrawn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
Frc Postec Plus
Generic name
Root canal post, preformed
Model / reference
603541AN
Primary DI / UDI-DI
DVIV603541AN1
FDA product code
ELR
GMDN term
Root canal post, preformed
Device class
Class I
Regulation number
872.3810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Root canal post, preformed

Similar devices in this category

Other devices filed under Root canal post, preformed.

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Properties

  • Single use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)