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Advance® KFDAN210

by MicroPort Orthopedics Inc.

Advance® KFDAN210 is a Class II device made by MicroPort Orthopedics Inc., listed in FDA GUDID since 20 Oct 2015 (UDI-DI M684KFDAN2101), 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 NumberM684KFDAN2101 UDI-DI Date20 Oct 2015ListedStatusListed 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  • Withdrawn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
Advance®
Generic name
Knee arthroplasty wedge
Model / Ref / Catalog
KFDAN210
Primary DI / UDI-DI
M684KFDAN2101
FDA product code
JWH
GMDN term
Knee arthroplasty wedge
Device class
Class II
Regulation number
888.3560
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Height — 10 Millimeter

Related devices

Category: Knee arthroplasty wedge

Similar devices in this category

Other devices filed under Knee arthroplasty wedge.

Other devices from MicroPort Orthopedics Inc.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)