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VertebraLINK 84-0505/0401

by Linkspine, Inc.

VertebraLINK 84-0505/0401 is a Class I device made by Linkspine, Inc., listed in FDA GUDID since 24 Apr 2018 (UDI-DI 00817329023555), 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 Number00817329023555 UDI-DI Date24 Apr 2018ListedStatusListed 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  • Withdrawn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
VertebraLINK
Generic name
Bone curette, reusable
Model / Ref / Catalog
84-0505/0401
Primary DI / UDI-DI
00817329023555
FDA product code
FZS
GMDN term
Bone curette, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone curette, reusable

Other devices from Linkspine, Inc.

See all devices from Linkspine, Inc. →

Properties

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