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Modulus Hip System Reamer

by Limacorporate 7 variants

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 Number08033390030724 UDI-DI Date15 Apr 2016ListedStatusListed 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  • Withdrawn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
Modulus Hip System
Generic Name
Medullary canal orthopaedic reamer, rigid
Model / Ref / Catalog
Reamer, 9043.10.200
Primary DI / UDI-DI
08033390030724
510(k) Number
FDA Product Code
KWY, LPH, JDI, KWZ
GMDN Term
Medullary canal orthopaedic reamer, rigid
Device Class
Class II
Regulation Number
888.3390, 888.3358, 888.3350, 888.3310
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Medullary canal orthopaedic reamer, rigid

Cleared under the same submission (K112158)

Show all (12)

Other devices from Limacorporate

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No