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LZI Oxycodone 300 Level 2 Control 0628

by Lin-Zhi International, Inc.

LZI Oxycodone 300 Level 2 Control 0628 is a Class I device made by Lin-Zhi International, Inc., listed in FDA GUDID since 19 Aug 2021 (UDI-DI B07606280), 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 NumberB07606280 UDI-DI Date19 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  • Withdrawn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 300 Level 2 Control
Generic name
Oxycodone IVD, control
Model / Ref / Catalog
0628
Description
5mL/bottle Concentration: 375 ng/mL of Oxycodone
Primary DI / UDI-DI
B07606280
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

Similar devices in this category

Other devices filed under 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)