Data / Medical devices / United Kingdom / Lockdown Medical Limited
Lockdown Medical Limited: FDA-registered device maker in Redditch Worcestershire, United Kingdom, 3 510(k) clearances
Lockdown Medical Limited is registered with the FDA (registration 8020712) in Redditch Worcestershire, United Kingdom. It lists 9 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 15, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8020712
- FEI number
- 3008237817
- Address
- 16 The Oaks Clews Road, Redditch Worcestershire, United Kingdom, B98 7ST
- Owner or operator
- Lockdown Medical Ltd (8020712)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 15, 2007
- Registered through
- 2026
- Brand names listed
- LockDown, Lockdown Depth Gauge
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bit, Drill | HTW | 1 | Manufacturer | accessdata.fda.gov |
| Fastener, Fixation, Nondegradable, Soft Tissue | MBI | 2 | Manufacturer | accessdata.fda.gov |
| Gauge, Depth | HTJ | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Ligature Passing And Knot Tying | HCF | 1 | Manufacturer | accessdata.fda.gov |
| Mesh, Surgical, Polymeric | FTL | 2 | Manufacturer | accessdata.fda.gov |
| Screwdriver | HXX | 1 | Manufacturer | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Manufacturer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Contract manufacturer | accessdata.fda.gov |
| Washer, Bolt Nut | HTN | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| February 15, 2011 | K091207 | SURGICRAFT LOCKDOWN ACROMIOCLAVICULAR (AC) DEVICE | HTN | Substantially Equivalent | Surgicraft , Ltd. | accessdata.fda.gov |
| July 24, 2008 | K072370 | SURGICRAFT SURGICAL MESH SYSTEM | FTL | Substantially Equivalent | Surgicraft , Ltd. | accessdata.fda.gov |
| June 13, 2008 | K080447 | SURGICRAFT SCREW FIXATION SYSTEM | MBI | Substantially Equivalent | Surgicraft , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Screwdriver
- All makers of Bit, Drill
- All makers of Instrument, Ligature Passing And Knot Tying
- All makers of Tape, Measuring, Rulers And Calipers
- All makers of Washer, Bolt Nut
- All makers of Mesh, Surgical, Polymeric
Updated February 15, 2011. 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.