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LZI Oxycodone 100 Level 2 Control 0618

by Lin-Zhi International, Inc.

LZI Oxycodone 100 Level 2 Control 0618 is a Class I device made by Lin-Zhi International, Inc., listed in FDA GUDID since 18 Aug 2021 (UDI-DI B07606180), 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 NumberB07606180 UDI-DI Date18 Aug 2021ListedStatusListed 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  • Withdrawn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
LZI Oxycodone 100 Level 2 Control
Generic name
Oxycodone IVD, control
Model / Ref / Catalog
0618
Description
5mL/bottle Concentration: 125 ng/mL of Oxycodone
Primary DI / UDI-DI
B07606180
FDA product code
LAS
GMDN term
Oxycodone IVD, control
Device class
Class I
Regulation number
862.3280
GUDID distribution status
In Commercial Distribution

Related devices

Category: Oxycodone IVD, control

Other devices from Lin-Zhi International, Inc.

See all devices from Lin-Zhi International, Inc. →

Properties

  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)