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Enduro NR871M

by Aesculap, Inc.

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Overview

ENDURO is a revolutionary rotating hinged total knee prosthesis designed to replace damaged or dysfunctional knee joints, providing unparalleled stability and mobility. With its unique mechanism and articulating components, ENDURO offers a safe and effective solution for patients undergoing knee replacement surgery.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046964010156 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: not 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  • Withdrawn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
Enduro
Generic Name
Rotating hinged total knee prosthesis
Model / Ref / Catalog
NR871M
Primary DI / UDI-DI
04046964010156
FDA Product Code
KRO
GMDN Term
Rotating hinged total knee prosthesis
Device Class
Class II
Regulation Number
888.3510
GUDID distribution status
Not in Commercial Distribution

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No