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419.96

by Synthes GmbH

419.96 (41996) is a Class II device made by Synthes GmbH, listed in FDA GUDID since 14 Sep 2015 (UDI-DI 10886982214805), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10886982214805 UDI-DI Date14 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Implantable bone nut
Model / Ref / Catalog
419.96, 41996
Primary DI / UDI-DI
10886982214805
FDA product code
HTN
GMDN term
Implantable bone nut
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Implantable bone nut

Similar devices in this category

Other devices filed under Implantable bone nut.

Other devices from Synthes GmbH

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  • 68.134.011

    Class II

  • Volt 68.134.111

    Class II

See all devices from Synthes GmbH →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (10, all answered No)