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Advantim® 18729100

by MicroPort Orthopedics Inc.

Advantim® 18729100 is a Class II device made by MicroPort Orthopedics Inc., listed in FDA GUDID since 23 Oct 2015 (UDI-DI M684187291001), 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 NumberM684187291001 UDI-DI Date23 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  • Withdrawn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
Advantim®
Generic name
Coated knee tibia prosthesis
Model / Ref / Catalog
18729100
Primary DI / UDI-DI
M684187291001
FDA product code
JWH
GMDN term
Coated knee tibia prosthesis
Device class
Class II
Regulation number
888.3560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Coated knee tibia prosthesis

Similar devices in this category

Other devices filed under Coated knee tibia prosthesis.

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)