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Benco 5899-058

by Benco Dental Supply Co.

Benco 5899-058 is a Class I device made by Benco Dental Supply Co., listed in FDA GUDID since 4 Aug 2022 (UDI-DI 00366975064806), 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 Number00366975064806 UDI-DI Date4 Aug 2022ListedStatusListed 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  • Withdrawn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
Benco
Generic name
Root canal post, preformed
Model / reference
5899-058
Primary DI / UDI-DI
00366975064806
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.

Other devices from Benco Dental Supply Co.

See all devices from Benco Dental Supply Co. →

Properties

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