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Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima KT77821

by Syneron Medical Ltd

Listed FDA GUDID listing, not in commercial distribution

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 Number17290109952724 UDI-DI Date31 Jan 2020ListedStatusListed GUDID: not 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  • Withdrawn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
Regular Internal Handpiece 5-Pack Sterile Single-Use, CO2RE Intima
Generic Name
Dermatological laser beam guiding handpiece
Model / Reference
KT77821
Primary DI / UDI-DI
17290109952724
510(k) Number
FDA Product Code
GEX
GMDN Term
Dermatological laser beam guiding handpiece
Device Class
Class II
Regulation Number
878.4810
GUDID distribution status
Not in Commercial Distribution

Related devices

Cleared under the same submission (K181523)

Show all (12)

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Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

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