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Hand Piece Internal hygienic, Packaged, CO2RE AS89733

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 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290109952376 UDI-DI Date9 Mar 2017ListedStatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Hand Piece Internal hygienic, Packaged, CO2RE
Generic Name
Dermatological carbon dioxide laser system
Model / Ref / Catalog
AS89733
Primary DI / UDI-DI
07290109952376
510(k) Number
FDA Product Code
GEX
GMDN Term
Dermatological carbon dioxide laser system
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

  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (11)

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