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Sterling 5259-507

by Benco Dental Supply Co. 2 variants

Sterling 5259-507 is a Class I device made by Benco Dental Supply Co., listed in FDA GUDID since 13 Dec 2023 (UDI-DI 00366975013040), 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 Number00366975013040 UDI-DI Date13 Dec 2023ListedStatusListed 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  • Withdrawn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
Sterling
Generic name
Fibreoptic dental light
Model / reference
5259-507
Primary DI / UDI-DI
00366975013040
FDA product code
EGS
GMDN term
Fibreoptic dental light
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Fibreoptic dental light

Similar devices

Also classified as Fibreoptic dental light.

Similar devices

Other devices filed under FDA product code EGS (Handpiece, Contra- And Right-Angle Attachment, Dental).

Other devices from Benco Dental Supply Co.

See all devices from Benco Dental Supply Co. →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)