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Data / Medical devices / United Kingdom / Riverside Medical Packaging Company Ltd

Riverside Medical Packaging Company Ltd: FDA-registered device maker in Derby Derbyshire, United Kingdom, 21 510(k) clearances

Riverside Medical Packaging Company Ltd is registered with the FDA (registration 3008559295) in Derby Derbyshire, United Kingdom. It lists 29 device types. The FDA files 21 510(k) clearances under its listings, the newest dated August 7, 2025. Registered through 2026. FDA data exported November 3, 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.

Get makers like this oneWatch Riverside Medical Packaging Company Ltd
FDA registration number
3008559295
Address
Newmarket Drive, Derby Derbyshire, United Kingdom, DE24 8SW
Owner or operator
Riverside Medical Packaging Company Ltd (10033563)
Roles
Contract manufacturer, Repackager or relabeler
First device listed
August 1, 2013
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Cannula, OphthalmicHMX1Repackager or relabeleraccessdata.fda.gov
Cannula, Ophthalmic, Posterior Capsular Polishing, Polyvinyl AcetalMXY1Repackager or relabeleraccessdata.fda.gov
Cannula, Surgical, General & Plastic SurgeryGEA1Repackager or relabeleraccessdata.fda.gov
Catheter, Retention Type, BalloonEZL2Contract manufactureraccessdata.fda.gov
Cerclage, FixationJDQ2Repackager or relabeleraccessdata.fda.gov
CystotomeHNY1Repackager or relabeleraccessdata.fda.gov
Device, Irrigation, Ocular SurgeryKYG1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, HydrophilicNAC1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, OcclusiveNAD1Repackager or relabeleraccessdata.fda.gov
Filler, Bone Void, Calcium CompoundMQV2Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Handpiece, Direct Drive, Ac-PoweredEKX1Repackager or relabeleraccessdata.fda.gov
Hemostatic Wound Dressing Without Thrombin Or Other BiologicsQSYURepackager or relabeleraccessdata.fda.gov
Implant, Endosseous, OrthodonticOAT2Repackager or relabeleraccessdata.fda.gov
Kit, Surgical Instrument, DisposableKDD1Repackager or relabeleraccessdata.fda.gov
Marker, ScleraHMQ1Repackager or relabeleraccessdata.fda.gov
Microtools, Assisted Reproduction (Pipettes), ExemptPUC2Repackager or relabeleraccessdata.fda.gov
Needle, Aspiration And Injection, DisposableGAA1Repackager or relabeleraccessdata.fda.gov
Pin, Fixation, SmoothHTY2Repackager or relabeleraccessdata.fda.gov
Pin, Fixation, ThreadedJDW2Repackager or relabeleraccessdata.fda.gov
Plate, Fixation, BoneHRS2Repackager or relabeleraccessdata.fda.gov
Probe, LachrymalHNL1Repackager or relabeleraccessdata.fda.gov
Probe, Radiofrequency LesionGXI2Repackager or relabeleraccessdata.fda.gov
Probe, Uptake, NuclearIZD1Repackager or relabeleraccessdata.fda.gov
Rod, Fixation, Intramedullary And AccessoriesHSB2Repackager or relabeleraccessdata.fda.gov
Screw, Fixation, BoneHWC2Repackager or relabeleraccessdata.fda.gov
Staple, Fixation, BoneJDR2Repackager or relabeleraccessdata.fda.gov
Strip, SchirmerKYD1Repackager or relabeleraccessdata.fda.gov
Surgical Smoke PrecipitatorPQM2Repackager or relabeleraccessdata.fda.gov
Washer, Bolt NutHTN2Repackager or relabeleraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
August 7, 2025K250622Succession™ AFN SystemHSBSubstantially EquivalentOrtho Solutions UK , Ltd.accessdata.fda.gov
February 23, 2024K240212COGNiTiON™ Staple SystemJDRSubstantially EquivalentOrtho Solutions UK , Ltd.accessdata.fda.gov
November 17, 2023K230589Celox Rapid X-Ray GauzeQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
December 30, 2021K212547Quick-Start ScrewsHWCSubstantially EquivalentInnovate Orthopaedics Limitedaccessdata.fda.gov
April 21, 2021K202639si-MochiMQVSubstantially EquivalentBiostone, Ltd.accessdata.fda.gov
November 20, 2020K202764Ortho Solutions Plating SystemHRSSubstantially EquivalentOrtho Solutions UK , Ltd.accessdata.fda.gov
March 8, 2017K163489OrthoSolutions 'System26' Bone ScrewsHWCSubstantially EquivalentOrtho Solutions UK Limitedaccessdata.fda.gov
December 20, 2016DEN150022Ultravision Visual Clearing SystemPQMUnknownAlesi Surgical, Ltd.accessdata.fda.gov
April 9, 2014K132401MEGA ISQEKXSubstantially EquivalentOsstell ABaccessdata.fda.gov
September 14, 2012K121575OXFORD ANKLE FUSION NAIL(AFN) SYSTEMHSBSubstantially EquivalentOrtho Solutions Limitedaccessdata.fda.gov
August 1, 2012K113560CELOX GAUZE PROQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
December 19, 2011K110895ORTHO SOLUTIONS TRAUMA IMPLANTS FOR OSTEOSYNTHESISHWCSubstantially EquivalentOrtho Solutions Limitedaccessdata.fda.gov
May 10, 2011K110386CELOX RAPID GAUZEQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
December 8, 2010K102965CELOX TRAUMA GAUZE AG, CELOX HEMOSTATIC ANTIBACTERIAL TRAUMA GAUZE, OMNI-STAT TRAUMA GAUZE AG, OMNI-STAT HEMOSTATIC ANTIQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
June 14, 2010K090608MINTA RYAN RF THERMOCOUPLE ELECTRODE (RYAN-50, 100, 150 AND 200), MINTA INTERMEDIATE CABLE (RYAN-C, -R, -B)GXISubstantially EquivalentMinta Medical Limitedaccessdata.fda.gov
April 1, 2010K100633INFINITAS MINI-IMPLANT MODEL: DB10-0009, DB10-0010,DB10-0012,DB10-0015,DB10-0016OATSubstantially EquivalentD B Orthodontics, Ltd.accessdata.fda.gov
January 20, 2010K093593CELOX PRO, CELOX PRO OTC, CELOX HEMOSTATIC GRANULES, CELOX PRO HEMOSTATIC GRANULES, OMNI STAT PROQSYSubstantially EquivalentMedtrade Products Limitedaccessdata.fda.gov
January 14, 2010K093519MEDTRADE PRODUCTS CELOX VASCULAR TOPICAL HEMOSTATIC GRANULES ON SHEETQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
July 9, 2008K080097MEDTRADE PRODUCTS CELOX HEMOSTATIC GRANULES ON SHEETQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov
October 26, 2007K072086INFINITAS MINI-IMPLANT SYSTEM/GUIDANCE SYSTEMOATSubstantially EquivalentD B Orthodontics, Ltd.accessdata.fda.gov
June 2, 2006K061079MEDTRADE PRODUCTS CELOX TOPICAL HEMOSTATIC GRANULES, MEDTRADE PRODUCTS CELOX 762 HEMOSTATIC GRANULESQSYSubstantially EquivalentMedtrade Products , Ltd.accessdata.fda.gov

Compare with other makers

Updated August 7, 2025. 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.