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Zavation 355-5560-1

by Zavation

Zavation 355-5560-1 is a Class II device made by Zavation, listed in FDA GUDID since 14 Dec 2023 (UDI-DI 00842166171923), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842166171923 UDI-DI Date14 Dec 2023ListedStatusListed 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  • Withdrawn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

Trade name
Zavation
Generic name
Orthopaedic bone screw (non-sliding)
Model / reference
355-5560-1
Primary DI / UDI-DI
00842166171923
FDA product code
NKB, KWQ
GMDN term
Orthopaedic bone screw (non-sliding)
Device class
Class II
Regulation number
888.3070, 888.3060
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Orthopaedic bone screw (non-sliding).

Other devices from Zavation

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Properties

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