Tomas Pin 6 MM

FDA 510(k) K062732 · Dentaurum

Substantially Equivalent

510(k) numberK062732

Submission

Device name
Tomas Pin 6 MM
Applicant
Dentaurum
Newtown, PA, US
Received
September 13, 2006
Decision date
October 25, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OAT – Implant, Endosseous, Orthodontic
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3640
Specialty
Dental
Implant
Yes

It is intended to provide a fixed anchorage point for attachment of orthodontic appliances to facilitate the orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has been completed.

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More from Syntec Scientific Corporation

510(k)DeviceDecision
K062733Tomas Pin SD 6, 8, and 10 MMOAT · Traditional 11/09/2006SE
K042965Tomas PinOAT · Traditional 04/15/2005SE
K030644Contec Duo, Contec LC, Contec LCRDYH · Traditional 11/21/2003SE
K032195Dentaurum Glastec Dental Orthodontic CementDYH · Traditional 10/07/2003SE
K030980Dentaurum No-Mix One Step Bracket AdhesiveDYH · Traditional 08/25/2003SE
K030977Dentaurum Mix Two-Paste Bracket AdhesiveDYH · Traditional 08/25/2003SE
K030641Contec LightEBZ · Traditional 06/10/2003SE
K011428TriceramEIH · Traditional 06/05/2001SE
K011425CarmenEIH · Traditional 06/05/2001SE

Questions and answers

When was Tomas Pin 6 MM cleared by the FDA?

Tomas Pin 6 MM (K062732) received a 510(k) decision of Substantially Equivalent on October 25, 2006, 42 days after the submission was received.

What is the product code of K062732?

The FDA product code is OAT – Implant, Endosseous, Orthodontic, a Class II (moderate risk) device regulated under 21 CFR 872.3640.