Skip to content

Ensizor ES26235

by Slater Endoscopy LLC

Ensizor ES26235 is a Class II device made by Slater Endoscopy LLC, listed in FDA GUDID since 23 Aug 2016 (UDI-DI M707ES26235), 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 NumberM707ES26235 UDI-DI Date23 Aug 2016ListedStatusListed 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  • Withdrawn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
Ensizor
Generic name
Flexible endoscopic scissors, single-use
Model / Ref / Catalog
ES26235
Primary DI / UDI-DI
M707ES26235
FDA product code
OCZ
GMDN term
Flexible endoscopic scissors, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Length — 235 Centimeter
Outer Diameter — 2.6 Millimeter

Related devices

Category: Flexible endoscopic scissors, single-use

Other devices from Slater Endoscopy LLC

See all devices from Slater Endoscopy LLC →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)