Data / Medical devices / United Kingdom / Morgan Steer Orthopaedics Ltd
Morgan Steer Orthopaedics Ltd: FDA-registered device maker in Leicester Leicestershire, United Kingdom, 4 510(k) clearances
Morgan Steer Orthopaedics Ltd is registered with the FDA (registration 3013438730) in Leicester Leicestershire, United Kingdom. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated August 22, 2013. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3013438730
- Address
- 9 Furnace House Narborough Wood Business Park, Desford Road, Enderby, Leicester Leicestershire, United Kingdom, LE19 4XT
- Owner or operator
- Morgan Steer Orthopaedics Ltd (10086241)
- Roles
- Specification developer
- First device listed
- October 25, 2022
- Registered through
- 2026
- Brand names listed
- CIQ SpineWand, CIQ System Controller, Cavity SpineWand, KNS-1706-10 - Crawford 17 ga x 6 Cannula, KNS-1904-10- DC 19 ga x 3 Cannula, Perc-D SpineWand, SCL600-01 - Crawford 17 ga x 6 cannula, SCL800-01- Crawford 17 ga x 8 cannula
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Specification developer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Specification developer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| August 22, 2013 | K132099 | ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND | GEI | Substantially Equivalent | ArthroCare Corporation | accessdata.fda.gov |
| January 15, 2010 | K091674 | ARTHROCARE COBLATOR IQ SYSTEM | GEI | Substantially Equivalent | Arthrocare Corp. | accessdata.fda.gov |
| April 27, 2007 | K063172 | ARTHROCARE CAVITY SPINEWAND | GEI | Substantially Equivalent | Arthrocare Corp. | accessdata.fda.gov |
| May 18, 2006 | K061259 | MODIFICATION TO ARTHROCARE PERC-D SPINEWAND | GEI | Substantially Equivalent | Arthrocare Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Cannula, Surgical, General & Plastic Surgery
Updated August 22, 2013. 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.