CoRoent 1689140

by NuVasive, LLC

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

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

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00887517163622 UDI-DI	Date24 Oct 2015Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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Withdrawn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: 1689140

Primary DI / UDI-DI: 00887517163622
FDA product code: MAX, PHM, OVD, MQP
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

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Properties

Sterilise before use
Implantable
Prescription use
Lot / batch number

Other properties (11)

Supplied sterile: No
Single use: No
Contains latex: No
Over-the-counter: No
Convenience kit: No
Combination product: No
HCT/P: No
Premarket exempt: No
Serial number: No
Expiration date: No
Manufacturing date: No