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Benco 4692-808

by Benco Dental Supply Co.

Benco 4692-808 is a Class II device made by Benco Dental Supply Co., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00366975002358), 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 Number00366975002358 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
Dental anaesthesia syringe, reusable
Model / reference
4692-808
Primary DI / UDI-DI
00366975002358
FDA product code
EJI
GMDN term
Dental anaesthesia syringe, reusable
Device class
Class II
Regulation number
872.6770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental anaesthesia syringe, reusable

Similar devices

Other devices filed under FDA product code EJI (Syringe, Cartridge).

Other devices from Benco Dental Supply Co.

See all devices from Benco Dental Supply Co. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)