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Nakoma 3100T-2400

by Alliance Partners LLC

Nakoma 3100T-2400 is a Class I device made by Alliance Partners LLC, listed in FDA GUDID since 23 Sep 2016 (UDI-DI M6863100T24000), 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 NumberM6863100T24000 UDI-DI Date23 Sep 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  • Withdrawn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
Nakoma
Generic name
Orthopaedic fixation implant alignment tool
Model / Ref / Catalog
3100T-2400
Primary DI / UDI-DI
M6863100T24000
FDA product code
LXH
GMDN term
Orthopaedic fixation implant alignment tool
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic fixation implant alignment tool

Similar devices in this category

Other devices filed under Orthopaedic fixation implant alignment tool.

Other devices from Alliance Partners LLC

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)