Rhenus Se & Co. Kg (foreign exporter, Holzwickede North Rhine-Westphalia, DE): 11 new FDA device listings, incl. introducer, catheter

Rhenus Se & Co. Kg (Holzwickede North Rhine-Westphalia, Delaware): 11 new FDA device listings, incl. introducer, catheter. Its amount of 11 is top-decile (93rd percentile of 2,709 records). Dated 186 days ago, it serves as a historical benchmark. Score 55/100. As of 2026-11-04, 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: 11 · 93th percentile of 2,709 DeviceEstablishmentPulse records · 5.5x the median

Free preview: all 15 published fields of this record are shown below. Locked: 39 related DE DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentRhenus Se & Co. Kg
Owner / operatorRhenus SE & Co. KG
RoleForeign exporter
Establishment typesExport Device to the United States But Perform No Other Operation on Device
LocationHolzwickede North Rhine-Westphalia, DE
New listings11
DevicesIntroducer, Catheter; Dilator, Vessel, For Percutaneous Catheterization; Stent, Iliac; Coronary Drug-Eluting Stent; Coronary Covered Stent; Stent, Superficial Femoral Artery; Catheter, Angioplasty, Peripheral, Transluminal; Catheter, Percutaneous; Stent, Coronary; Catheters, Transluminal Coronary Angioplasty, Percutaneous
Product codesDYB, DRE, NIO, NIQ, NIV, NIP, LIT, DQY, MAF, LOX
Device classesClass II, Class III, f
Medical specialtiesCardiovascular
Brand namesFORTRESS; ASTRON; ORSIRO MISSION; PAPYRUS; Pulsar-18 T3; Passeo-35 HP; PRO-Kinetic Energy; Passeo-18
First new listing2026-05-05
Latest new listing2026-05-05
FDA registration number3014656749
Registration expires2026-12-31
amount percentile93th of 2,709 (median 2, 5.5x 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: 2026-05-05
  • Data refreshed: 2026-11-04
  • Refunds on request within 14 days

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Top DeviceEstablishmentPulse records (DE first): Titanlinks Logistics LLC (repackager or relabeler, Newark, D · Titanlinks Logistics LLC (repackager or relabeler, Newark, D · Karl Storz Se & Co Kg (specification developer, TUTTLINGEN B · Karl Storz Se & Co Kg (specification developer, TUTTLINGEN B · Medi.Plan GmbH & Co. Kg (foreign exporter, Dortmund North Rh · Browse all by state and category →

LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 21:52:36 GMT

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Peer benchmark and outreach value: Rhenus Se & Co. Kg and 40 Delaware peers

  • Delaware DeviceEstablishmentPulse records like this one: 40
  • Rhenus Se & Co. Kg's amount: 93rd percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Delaware peer: $8,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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55 / 100 Score

  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Rhenus Se & Co. Kg in Holzwickede North Rhine-Westphalia, Delaware?

Rhenus Se & Co. Kg (Holzwickede North Rhine-Westphalia, DE), a foreign exporter, added 11 FDA device listings on 2026-05-05.

How does Rhenus Se & Co. Kg compare to other Delaware DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 11 is 5.5x the median of 2 across 2,709 records. It is 186 days old; check the official source for later updates before acting.

Rhenus Se & Co. Kg vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Rhenus Se & Co. KgHolzwickede North Rhine-Westphalia, DE1193rd2026-05-05
Mka Medikal Ic Ve Dis Ticaret Sanayi Limited SirketiCankaya Ankara, TR992nd2026-10-17
Kash Sales Inc.Richmond Hill Ontario, CA890th2026-10-16
Imperial Optical, IncTown Of Mount Royal, Quebec, CA377th2026-10-22

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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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