Data / Medical devices / United Kingdom / Loudwater Trade Finance Ltd
Loudwater Trade Finance Ltd: FDA-registered device maker in LONDON England, United Kingdom, 9 510(k) clearances
Loudwater Trade Finance Ltd is registered with the FDA (registration 3012026312) in LONDON England, United Kingdom. It lists 17 device types. The FDA files 9 510(k) clearances under its listings, the newest dated March 20, 2019. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3012026312
- Address
- 56a Crewys Road, LONDON England, United Kingdom, NW2 2AD
- Owner or operator
- LOUDWATER TRADE FINANCE LTD (10084061)
- Roles
- Contract sterilizer, Exporter to the US
- First device listed
- September 13, 2023
- Registered through
- 2027
- Brand names listed
- BOTTLE, COLLECTION, VACUUM, Catheter, Drape, surgical, MOUTHPIECE, BREATHING, SPIROMETER, DIAGNOSTIC, Shiley Cuffed Tracheostomy Tube 4CN65A, Shiley Cuffed Tracheostomy Tube 5CN70A, Shiley Disposable Inner Cannula 4IC65 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 |
|---|---|---|---|---|---|---|
| March 20, 2019 | K183399 | BD Nexiva Closed IV Catheter System | FOZ | Substantially Equivalent | Becton Dickinson Infusion Therapy Systems, Inc. | accessdata.fda.gov |
| February 24, 2015 | K142296 | Shiley Adult Flexible Tracheostomy Tube Cuffless, Disposable Inner Cannula; Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, Disposable Inner Cannula | JOH | Substantially Equivalent | Covidien | accessdata.fda.gov |
| November 9, 2010 | K102666 | KIMBERLY-CLARK SURGICAL DRAPES WITH AAMI LIQUID BARRIER LEVEL 4 CLAIM | KKX | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| August 3, 2007 | K063835 | ALLEVYN AG DRESSING | FRO | Substantially Equivalent | Smith & Nephew, Inc. | accessdata.fda.gov |
| June 16, 2005 | K051416 | SHILEY TRACHEOSOFT XLT EXTENDED LENGTH TRACHEOSTOMY TUBE AND INNER CANNULA | JOH | Substantially Equivalent | Mallinckrodt Medical | accessdata.fda.gov |
| July 13, 1994 | K942779 | DISPOSABLE BACTERIOLOGICAL FILTER | BZG | Substantially Equivalent | Vitalograph, Inc. | accessdata.fda.gov |
| August 3, 1989 | K893900 | PRIMAPORE I.V. | KGX | Substantially Equivalent for Some Indications | Smith & Nephew United, Inc. | accessdata.fda.gov |
| July 23, 1985 | K852211 | OPSITE WOUND DRESSING | NAD | Substantially Equivalent for Some Indications | Smith & Nephew, Inc. | accessdata.fda.gov |
| June 26, 1981 | K811447 | SHILEY DISPOSABLE CANNULA TRACH. TUBE | BTO | Substantially Equivalent | Shiley, Inc. | accessdata.fda.gov |
Compare with other makers
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Updated March 20, 2019. 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.