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Two Striper SNOWLIGHT REFILL- 1.4MM 10 PCS

by Abrasive Technology LLC

Two Striper SNOWLIGHT REFILL- 1.4MM 10 PCS (C831003) is a Class I device made by Abrasive Technology LLC, listed in FDA GUDID since 25 May 2021 (UDI-DI B868C8310031), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB868C8310031 UDI-DI Date25 May 2021ListedStatusListed 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  • Withdrawn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
Two Striper
Generic name
Root canal post, preformed
Model / Ref / Catalog
SNOWLIGHT REFILL- 1.4MM 10 PCS, C831003
Primary DI / UDI-DI
B868C8310031
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 Abrasive Technology LLC

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Properties

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