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Kakusan kks-225

by SZ KKS Silicone&Electronic Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number06980088700006 UDI-DI Date13 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Kakusan
Generic Name
Blue/red/infrared phototherapy lamp
Model / Reference
kks-225
Primary DI / UDI-DI
06980088700006
510(k) Number
FDA Product Code
OHS
GMDN Term
Blue/red/infrared phototherapy lamp
Device Class
Class II
Regulation Number
878.4810
GUDID distribution status
In Commercial Distribution
Sterilization Method
Liquid Chemical

Related devices

Cleared under the same submission (K254007)

Other devices from SZ KKS Silicone&Electronic Co., Ltd.

Properties

  • Manufacturing Date

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No