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Lineage 36510046

by MicroPort Orthopedics Inc.

Lineage 36510046 is a Class II device made by MicroPort Orthopedics Inc., listed in FDA GUDID since 20 Oct 2015 (UDI-DI M684365100461), 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 NumberM684365100461 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  • Withdrawn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
Lineage
Generic name
Metallic acetabulum prosthesis
Model / Ref / Catalog
36510046
Primary DI / UDI-DI
M684365100461
FDA product code
LPH
GMDN term
Metallic acetabulum prosthesis
Device class
Class II
Regulation number
888.3358
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 46 Millimeter

Related devices

Category: Metallic acetabulum prosthesis

Other devices from MicroPort Orthopedics Inc.

See all devices from MicroPort Orthopedics Inc. →

Properties

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