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EZflex Lidocaine 4% & Menthol 1% pain relief patch 5 count

by Care Living Diagnostics Inc

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00383568101625 UDI-DI Date4 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Transdermal medication patch
Model / Ref / Catalog
1
Primary DI / UDI-DI
00383568101625
FDA Product Code
OMW
GMDN Term
Transdermal medication patch
Device Class
Class I
Regulation Number
890.5710
GUDID distribution status
In Commercial Distribution

Other devices from Care Living Diagnostics Inc

See all devices from Care Living Diagnostics Inc →

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No