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EndoWrist 381127

by Intuitive Surgical, Inc.

EndoWrist 381127 is a Class II device made by Intuitive Surgical, Inc., listed in FDA GUDID since 8 Jul 2016 (UDI-DI 00886874110904), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00886874110904 UDI-DI Date8 Jul 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  • Withdrawn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
EndoWrist
Generic name
Endoscopic motorized cutting stapler, single-use
Model / reference
381127
Primary DI / UDI-DI
00886874110904
FDA product code
NAY
GMDN term
Endoscopic motorized cutting stapler, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic motorized cutting stapler, single-use

Similar devices in this category

Other devices filed under Endoscopic motorized cutting stapler, single-use.

Other devices from Intuitive Surgical, Inc.

See all devices from Intuitive Surgical, Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)