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PRECICE® Intramedullary Limb Lengthening System Instrument RMR1-120

by Nuvasive Specialized Orthopedics, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812258026707 UDI-DI Date5 Feb 2016ListedStatusListed 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  • Withdrawn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
PRECICE® Intramedullary Limb Lengthening System Instrument
Generic Name
Medullary canal orthopaedic reamer, flexible
Model / Ref / Catalog
RMR1-120
Primary DI / UDI-DI
00812258026707
FDA Product Code
HTO
GMDN Term
Medullary canal orthopaedic reamer, flexible
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Medullary canal orthopaedic reamer, flexible

Other devices from Nuvasive Specialized Orthopedics, Inc.

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Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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