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PeriOptix A-LED5-99

by Den-Mat Holdings, LLC GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00359883007447 UDI-DIDate23 Sep 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
PeriOptix
Generic Name
LED dental light, battery-powered
Model / Reference
A-LED5-99
Primary DI / UDI-DI
00359883007447
FDA Product Code
KYT
GMDN Term
LED dental light, battery-powered
Device Class
Class I
Regulation Number
880.6350
GUDID distribution status
In Commercial Distribution

Other devices from Den-Mat Holdings, LLC

See all devices from Den-Mat Holdings, LLC →

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Serial Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No