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Deka Smartxide 50 M079AL1

by El.en. SpA

Deka Smartxide 50 M079AL1 is a Class II device made by El.en. SpA, cleared under FDA 510(k) K072159 on 27 Dec 2007 and listed in FDA GUDID since 13 Sep 2016 (UDI-DI 08057017760085), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K072159

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08057017760085 UDI-DI Date13 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK072159 Date27 Dec 2007DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K072159 decided 27 Dec 2007 Active
  • FDA GUDID UDI-DI 08057017760085 listed 13 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K072159
  2. Listed FDA GUDID 08057017760085

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Deka Smartxide 50
Generic name
Dermatological carbon dioxide laser system
Model / Ref / Catalog
M079AL1
Primary DI / UDI-DI
08057017760085
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
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code GEX (Powered Laser Surgical Instrument).

Other devices from El.en. SpA

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)