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Perioscan, Model: D 3496

by SIRONA Dental Systems GmbH

510(k) K072107

Perioscan, Model: D 3496 is a Class II device made by SIRONA Dental Systems GmbH, cleared under FDA 510(k) K072107 on 14 Feb 2008, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK072107 Date14 Feb 2008ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
ELC
Device class
Class II
Regulation
21 CFR Part 872.4850
Advisory committee
Dental
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code ELC (Scaler, Ultrasonic).

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