MedSource Labs, LLC (manufacturer, Chanhassen, MN): 4 new FDA device listings, incl. catheter, intravascular, therapeutic, short-term less than 30 days

MedSource Labs, LLC (Chanhassen, Minnesota): 4 new FDA device listings, incl. catheter, intravascular, therapeutic, short-term less than 30 days. Its amount of 4 is above the median of 1 (83rd percentile). Dated 113 days ago, it serves as a historical benchmark. Score 85/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 42 related MN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentMedSource Labs, LLC
Owner / operatorMedsource Labs, LLC
RoleManufacturer
Establishment typesDevelop Specifications But Do Not Manufacture At This Facility; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
LocationChanhassen, MN, US
New listings4
DevicesCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days; General Purpose Dental Tray; Clinical Electronic Thermometer
Product codesFOZ, OFX, SDV
Device classesClass I, Class II
Medical specialtiesGeneral Hospital, Dental
Brand namesClearSafe Closed System; Dental Kit; CLINICAL INFRARED THERMOMETERS; MedSource QuickSafe Safety IV Catheter; MedSource Passivo IV Safety Catheter; MedSource PurSafe Safety IV Catheter
First new listing2026-06-10
Latest new listing2026-07-14
FDA registration number3003674698
Registration expires2026-12-31
amount percentile83th of 2,570 (median 1, 4.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-07-14
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: MedSource Labs, LLC and 43 Minnesota peers

  • Minnesota DeviceEstablishmentPulse records like this one: 43
  • MedSource Labs, LLC's amount: 83rd percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Minnesota peer: $8,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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85 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for MedSource Labs, LLC in Chanhassen, Minnesota?

MedSource Labs, LLC (Chanhassen, MN), a manufacturer, added 4 FDA device listings between 2026-06-10 and 2026-07-14.

How does MedSource Labs, LLC compare to other Minnesota DeviceEstablishmentPulse records?

Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 113 days old; check the official source for later updates before acting. Its Score of 85/100 puts it among the stronger signals in this feed.

MedSource Labs, LLC vs. top 2 peers

OrganizationLocationAmountPercentileRecord date
MedSource Labs, LLCChanhassen, MN483rd2026-07-14
Piraeus Medical, Inc.Maple Grove, MN483rd2026-10-12
Boston Scientific CorporationSaint Paul, MN2498th2026-10-16

Related records

DeviceEstablishmentPulse: Manufacturer DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Minnesota

Cross-dataset signals in Minnesota

FdaApprovalPulse: records in Minnesota (61)

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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.

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