Star Titan Series Motors & Attachments
FDA 510(k) K960260 · Dentalez Group
510(k) numberK960260
Submission
- Device name
- Star Titan Series Motors & Attachments
- Applicant
- Dentalez Group
Lancaster, PA, US - Received
- January 18, 1996
- Decision date
- March 28, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K101172 | RDT3 Handpiece Head Model RDT3EFA · Traditional | Redent Nova, Ltd. | 07/27/2010SE |
| K093894 | Anthogyr Impulsion Implantology Contra-AngleEFA · Special | Anthogyr | 03/03/2010SE |
| K092446 | Intra Lux Head 3 LdsyEFA · Traditional | Kaltenbach & Voigt GmbH & Co. | 11/03/2009SE |
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| K092412 | Strong Implant HandpiecesEFA · Traditional | Saeshin Precision Co., Ltd. | 09/03/2009SE |
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More from Est. Anthogyr
| 510(k) | Device | Decision |
|---|---|---|
| K030133 | Solara Series Comprised of the Solara High Speed Dental Handpiece and the Solara Plus…EBF · Traditional | 04/29/2003SE |
| K021378 | Portable HDX Intraoral X-RayEHD · Traditional | 06/07/2002SE |
| K990844 | Stardental Axcs Sterile Water SystemEIA · Traditional | 05/28/1999SE |
| K983574 | Stardental Titan 3 Lubefree Motor AttachmentsEGS · Traditional | 01/08/1999SE |
| K982593 | Lube Free Autochuck Turbine with Vortex Air Seal for Use with Star Dental 430 Series…EFB · Traditional | 10/22/1998SE |
| K960719 | Star Dental 430 Series High Speed HandpieceEFA · Traditional | 03/28/1996SE |
| K960507 | Star Dental Pushbutton Autochuck Replacement Turbine for Midwest HandpiecesEFA · Traditional | 03/28/1996SE |
| K925567 | E 4000 Dental Operating ChairKLC · Traditional | 03/10/1994SE |
| K931093 | Quick-Connect 360 Swivel Tip Autoclavable SyringeEIA · Traditional | 01/21/1994SE |
| K902402 | High Speed Non-Fiber Optic Swivel HandpieceEBF · Traditional | 08/29/1990SE |
Questions and answers
When was Star Titan Series Motors & Attachments cleared by the FDA?
Star Titan Series Motors & Attachments (K960260) received a 510(k) decision of Substantially Equivalent on March 28, 1996, 70 days after the submission was received.
What is the product code of K960260?
The FDA product code is EFA – Handpiece, Belt And/Or Gear Driven, Dental, a Class I (low risk) device regulated under 21 CFR 872.4200.