Where does the data come from?

openFDA device registration and listing endpoint (U.S. Food and Drug Administration). Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm

Karl Storz Se & Co. Kg (contract manufacturer, NEUHAUSEN OBECK Baden-Wurttemberg, DE): 1 new FDA device listing, incl. endoscopic grasping/cutting instrument, non-powered

Q: How to monitor Karl Storz Se & Co. Kg and peer contract manufacturer records

DeviceEstablishmentPulse lists new DeviceEstablishmentPulse records from openFDA device registration and listing endpoint (U.S. Food and Drug Administration) as they are published; a free weekly email digest and paid alerts follow Delaware records like this one.

Karl Storz Se & Co. Kg (NEUHAUSEN OBECK Baden-Wurttemberg, Delaware): 1 new FDA device listing, incl. endoscopic grasping/cutting instrument, non-powered. Its amount of 1 is above the median of 2 (50th percentile). Dated 141 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 2026-11-04 · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 1 · 50th percentile of 2,709 DeviceEstablishmentPulse records · 0.5x 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.

Field	Value
Establishment	Karl Storz Se & Co. Kg
Owner / operator	Karl Storz Se & Co Kg
Role	Contract manufacturer
Establishment types	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	NEUHAUSEN OBECK Baden-Wurttemberg, DE
New listings	1
Devices	Endoscopic Grasping/Cutting Instrument, Non-Powered
Product codes	OCZ
Device classes	Class II
Medical specialties	Gastroenterology, Urology
Brand names	KARL STORZ Endoscopic Accessories for Urology
First new listing	2026-06-17
Latest new listing	2026-06-17
FDA registration number	3010707607
Registration expires	2027-12-31
amount percentile	50th of 2,709 (median 2, 0.5x median)
Peer records CSV (40 DE records)	🔒 Click to unlock →
CRM-ready export with official source URLs	🔒 Click to unlock →

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Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
Record date: 2026-06-17
Data refreshed: 2026-11-04
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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: Karl Storz Se & Co. Kg and 40 Delaware peers

Your role Typical deal size (USD) Assumed reply-to-deal rate (%)

Delaware DeviceEstablishmentPulse records like this one: 40
Karl Storz Se & Co. Kg's amount: 50th 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)

55 / 100 Score

Contract manufacturer or sterilizer adding work.
Class II or III devices: QMS and regulatory demands.

What is the DeviceEstablishmentPulse record for Karl Storz Se & Co. Kg in NEUHAUSEN OBECK Baden-Wurttemberg, Delaware?

Karl Storz Se & Co. Kg (NEUHAUSEN OBECK Baden-Wurttemberg, DE), a contract manufacturer, added 1 FDA device listing on 2026-06-17.

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

Its amount of 1 sits in the upper half (50th percentile) of 2,709 records; the median is 2. It is 141 days old; check the official source for later updates before acting.

Karl Storz Se & Co. Kg vs. top 3 peers

Organization	Location	Amount	Percentile	Record date
Karl Storz Se & Co. Kg	NEUHAUSEN OBECK Baden-Wurttemberg, DE	1	50th	2026-06-17
Tecomet Inc.	Wilmington, MA	3	77th	2026-10-15
Bard Shannon Limited	Humacao, PR	3	77th	2026-10-14
Orchid Orthopedic Solutions Oregon, Inc.	Oregon City, OR	3	77th	2026-10-05

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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.