Skip to content

Lazic 46.310

by Peter Lazic GmbH

Lazic 46.310 is a Class I device made by Peter Lazic GmbH, listed in FDA GUDID since 5 Aug 2020 (UDI-DI 04250603713654), 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 Number04250603713654 UDI-DI Date5 Aug 2020ListedStatusListed 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  • Withdrawn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
Lazic
Generic name
Bone hook
Model / Ref / Catalog
46.310
Primary DI / UDI-DI
04250603713654
FDA product code
GDG
GMDN term
Bone hook
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone hook

Similar devices in this category

Other devices filed under Bone hook.

Other devices from Peter Lazic GmbH

See all devices from Peter Lazic GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)