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ANODYNE Plate System 20140-16

by Corelink LLC

ANODYNE Plate System 20140-16 is a Class II device made by Corelink LLC, listed in FDA GUDID since 21 Jan 2016 (UDI-DI M7252014016), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM7252014016 UDI-DI Date21 Jan 2016ListedStatusListed GUDID: 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  • Withdrawn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
ANODYNE Plate System
Generic name
Bone-screw internal spinal fixation system, non-sterile
Model / Ref / Catalog
20140-16
Description
ANODYNE CERVICAL SCREW - VARIABLE SELF DRILLING - 4.0MM X 16MM
Primary DI / UDI-DI
M7252014016
FDA product code
KWQ
GMDN term
Bone-screw internal spinal fixation system, non-sterile
Device class
Class II
Regulation number
888.3060
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 16 Millimeter
Outer Diameter — 4 Millimeter

Related devices

Category: Bone-screw internal spinal fixation system, non-sterile

Other devices from Corelink LLC

See all devices from Corelink LLC →

Properties

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