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Organization (Industry)

Medela (Switzerland)

ClinicalTrials.gov lists Medela (Switzerland) as lead sponsor of 10 trials.

CH Industry Manufacturer
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3 0 2009 2026

Trials started per year with this organization as sponsor or collaborator, 1990 onward. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.

2026 is partial: 0 registered with a 2026 start date. The dashed outline is the pace from the 0 registered with a start date through September, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 0.4 trial starts a year over the five years to September, under the 5 a year the method needs.

This page covers Medela (Switzerland): 10 lead-sponsored trials and 1 legal-entity registration.

Get the Medela (Switzerland) report as a PDF

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Disease areas (11)

Shown in this order: most trials first.

Disease areas
Disease area Trials
Diabetes Mellitus 2
Diabetic Foot 2
Diabetic Neuropathies 2
Pressure Ulcer 2
Carcinoma, Non-Small-Cell Lung 1

Trials by start year as sponsor or collaborator (13)

Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.

Show the table of trials by start year as sponsor or collaborator
Trials by start year as sponsor or collaborator
Year Trials started
2024 1
2023 1
2021 1
2020 2
2019 1
2018 2
2017 1
2016 2
2015 3
2014 1

Recruitment duration, a model prediction: none of the 10 trials evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

Sponsor delivery record (1)

Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.

Sponsor delivery record
Enrollment Timeline
4 of 4 hit target (n=4) 2 of 4 on time (n=4)

Journals published in (10)

Shown in this order: most published in first.

Journals published in
Journal Publications
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 4
The Annals of thoracic surgery 4
Thoracic surgery clinics 2
Acta obstetricia et gynecologica Scandinavica 1
Chest 1

US granted patents (1)

Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.

US granted patents
US patents granted Granted in the last 5 years Most recent grant
295 35 2025-12-30

FDA recalls (4)

Shown in this order: most recent first.

FDA recalls
Product Classification Initiated
Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086 Software Version: N/A Product Description: Enteral Extension Set, Length 60 Orange-Striped Minibore Tubing, (Approx. Priming Vol. 2.00 mL), ENFit¿ Component: N/A Class II 2026-06-05
Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) SKU # 0876224. The Invia Foam Dressing Kit with FitPad consists of a foam pad, a section interface (Invia FitPad) and Transparent Film (one or more pieces depending on the kit size). Class II 2019-12-02
Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100 Class III 2018-12-05
Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model 087.4010); b. 15 Days Negative Pressure Wound Therapy (Model 087.4012); c. 60 Days Negative Pressure Wound Therapy (Model 087.4014); d. Endure Negative Pressure Wound Therapy (Model 087.4020 ); e. 15 Days Negative Pressure Wound Therapy (Model 087.4022); f. 60 Days Negative Pressure Wound Therapy (Model 087.4024). Product Usage: The Invia Motion Negative Pressure Wound Therapy (NPWT) system is indicated for patients who would benefit from a suction device (NPWT) as it creates an environment that promotes wound healing by secondary or tertiary (delayed primary) intention by preparing the wound bed for closure, reducing edema, promoting granulation tissue formation and perfusion, and by removing exudate and infectious material. Class II 2018-02-07

FDA import refusals (1)

FDA import refusals
Refused import lines Latest refusal
1 2017-01-23

Manufacturing and distribution sites (1)

Manufacturing and distribution sites
Facility Location Regulators Member organization
MEDELA AG BAAR Zug, CH FDA

Organization relationships (1)

Organization relationships
Related organization Relationship Evidence
Copenhagen University Hospital, Rigshospitalet Co sponsors trial with 1

Latest dated events (318)

Shown in this order: newest first.

Latest dated events
Date Event Source
2026-06-05 FDA recall FDA enforcement (warning and untitled letters, recalls, inspections, import refusals, debarment)
2025-12-30 Patent granted Granted US patents (PatentsView / USPTO)
2025-04-15 Patent granted Granted US patents (PatentsView / USPTO)
2024-11-05 Patent granted Granted US patents (PatentsView / USPTO)
2024-10-15 Patent granted Granted US patents (PatentsView / USPTO)

Biomarker capability evidence (2)

Shown in this order: tier desc, then gene symbol.

Biomarker capability evidence
Gene Role Evidence
ERAS Trial collaborator Named in trial inclusion criteria
ERAS Trial collaborator Mentioned in trial text

Not on this page

Checked, with nothing recorded for this organization: companies grouped under this page, related companies not grouped here, active development programs, approved assets, sec-reported annual financials, financing and grant events, fda warning letters, fda untitled letters, fda inspection record, climate targets, as filed, workforce and board diversity, as filed, clia clinical laboratory certificates, and biomarkers this organization publishes on.