Skip to content

Surtex RST-EL3

by Dentatus AB

Surtex RST-EL3 is a Class I device made by Dentatus AB, listed in FDA GUDID since 20 Jan 2025 (UDI-DI 07350081492380), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07350081492380 UDI-DI Date20 Jan 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Surtex
Generic name
Root canal post, preformed
Model / Ref / Catalog
RST-EL3
Primary DI / UDI-DI
07350081492380
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
Liquid Chemical
Size
Outer Diameter — 1.35 Millimeter
Length — 14.2 Millimeter

Related devices

Category: Root canal post, preformed

Similar devices in this category

Other devices filed under Root canal post, preformed.

Other devices from Dentatus AB

See all devices from Dentatus AB →

Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)