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MobileLink Acetabular Cup System 183-310/74

by WALDEMAR LINK GmbH & Co. KG

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04026575190744 UDI-DI Date9 Sep 2019ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
MobileLink Acetabular Cup System
Generic Name
Acetabular shell
Model / Ref / Catalog
183-310/74
Primary DI / UDI-DI
04026575190744
510(k) Number
FDA Product Code
LPH, MEH, LZO, OQG
GMDN Term
Acetabular shell
Device Class
Class II
Regulation Number
888.3358, 888.3353
GUDID distribution status
In Commercial Distribution

Related devices

Category: Acetabular shell

Cleared under the same submission (K182321)

Show all (12)

Other devices from WALDEMAR LINK GmbH & Co. KG

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Properties

  • Sterile
  • Implantable
  • Prescription Use
  • Serial Number
  • Expiration Date

Other properties (9)

  • Single Use: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Manufacturing Date: No