Data / Medical devices / United States / Silony Spine Corporation
Silony Spine Corporation: FDA-registered device maker in Doral, FL, United States, 20 510(k) clearances
Silony Spine Corporation is registered with the FDA (registration 3013422238) in Doral, FL, United States. It lists 11 device types. The FDA files 20 510(k) clearances under its listings, the newest dated June 26, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013422238
- Address
- 8200 NW 27th Street Suite #104, Doral, FL, United States, 33122
- Owner or operator
- Silony Medical GmbH (10054311)
- Roles
- Complaint file establishment
- First device listed
- March 21, 2017
- Registered through
- 2026
- Brand names listed
- (Re-)Positioning Tools, Adapter, CERVICAL CAGE, Control Gauges, Counter Torque, Dilatator, Distractor, Drill Guide and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 26, 2026 | K253921 | VERTICALE® Navigation Instruments | OLO | Substantially Equivalent | Silony Medical GmbH | accessdata.fda.gov |
| February 19, 2026 | K254148 | VERTICALE GPS Instruments | OLO | Substantially Equivalent | Silony Medical GmbH | accessdata.fda.gov |
| May 8, 2018 | K173347 | STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX | MAX | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| June 8, 2017 | K171112 | Trifore(tm) Cervical Plating System | KWQ | Substantially Equivalent | Neurostructures, Inc. | accessdata.fda.gov |
| December 1, 2015 | K152211 | PCT System | NKG | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| June 24, 2015 | K150053 | STALIF C; STALIF C-Ti | OVE | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| June 8, 2015 | K150643 | Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti | OVD | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| November 7, 2014 | K141942 | MIDLINE II TI | OVD | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| October 24, 2014 | K142079 | STALIF CTI, STALIF C | OVE | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| May 8, 2014 | K133200 | STALIF C(R) | OVE | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| January 9, 2014 | K133286 | MIDLINE (TM) | OVD | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| August 28, 2013 | K130461 | STALIF X | OVD | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| August 31, 2012 | K120819 | STALIF C | OVE | Substantially Equivalent | Centinel Spine, Inc. | accessdata.fda.gov |
| August 30, 2012 | K122444 | CERVICAL CAGE | ODP | Substantially Equivalent | Eisertech, LLC | accessdata.fda.gov |
| July 22, 2011 | K110915 | CERVICAL CAGE | ODP | Substantially Equivalent | Eisertech, LLC | accessdata.fda.gov |
| September 24, 2010 | K101301 | STALIF MIDLINE | MAX | Substantially Equivalent | Centinel Spine | accessdata.fda.gov |
| June 4, 2008 | K073109 | STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM | OVD | Substantially Equivalent | Surgicraft , Ltd. | accessdata.fda.gov |
| January 25, 2008 | K072415 | STALIF (TM) C | OVE | Substantially Equivalent | Surgicraft , Ltd. | accessdata.fda.gov |
| June 29, 2005 | K051027 | STALIF TT | MQP | Substantially Equivalent | Surgicraft , Ltd. | accessdata.fda.gov |
| September 8, 2004 | K041617 | STALIF TT | MQP | Substantially Equivalent | Surgicraft , Ltd. | accessdata.fda.gov |
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Updated June 26, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.