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Prime P2LESC36

by MicroPort Orthopedics Inc.

Prime P2LESC36 is a Class II device made by MicroPort Orthopedics Inc., listed in FDA GUDID since 5 Oct 2018 (UDI-DI M684P2LESC361), 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 NumberM684P2LESC361 UDI-DI Date5 Oct 2018ListedStatusListed 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  • Withdrawn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
Prime
Generic name
Non-constrained polyethylene acetabular liner
Model / Ref / Catalog
P2LESC36
Primary DI / UDI-DI
M684P2LESC361
FDA product code
LPH, OQG
GMDN term
Non-constrained polyethylene acetabular liner
Device class
Class II
Regulation number
888.3358
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 36 Millimeter

Related devices

Category: Non-constrained polyethylene acetabular liner

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)