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CoRoent 5150342

by NuVasive, LLC

CoRoent 5150342 is a Class II device made by NuVasive, LLC, listed in FDA GUDID since 11 Nov 2015 (UDI-DI 00887517637864), 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 Number00887517637864 UDI-DI Date11 Nov 2015ListedStatusListed 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  • Withdrawn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
CoRoent
Generic name
Polymeric spinal interbody fusion cage
Model / reference
5150342
Primary DI / UDI-DI
00887517637864
FDA product code
PHM, MQP, MAX, OVD
GMDN term
Polymeric spinal interbody fusion cage
Device class
Class II
Regulation number
888.3080, 888.3060
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Polymeric spinal interbody fusion cage

Other devices from NuVasive, LLC

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    Class II

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    Class II

  • ReLine 3800240

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See all devices from NuVasive, LLC →

Properties

  • Sterilise before use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)