Draegerwerk AG & Co. KGaA (manufacturer, LUEBECK Schleswig-Holstein, DE): 5 new FDA device listings, incl. support, breathing tube
Draegerwerk AG & Co. KGaA (LUEBECK Schleswig-Holstein, Delaware): 5 new FDA device listings, incl. support, breathing tube. Its amount of 5 is above the median of 1 (87th percentile). Dated 90 days ago, it serves as a historical benchmark. Score 75/100. 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: 5 · 87th percentile of 2,570 DeviceEstablishmentPulse records · 5.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 36 related DE DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Draegerwerk AG & Co. KGaA |
| Role | Manufacturer |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device |
| Location | LUEBECK Schleswig-Holstein, DE |
| New listings | 5 |
| Devices | Support, Breathing Tube; Warmer, Infant Radiant; Bilirubin (Total And Unbound) In The Neonate Test System; Ventilator, Continuous, Facility Use; Gas-Machine, Anesthesia |
| Product codes | JAY, FMT, MQM, CBK, BSZ |
| Device classes | Class I, Class II |
| Medical specialties | Anesthesiology, General Hospital, Clinical Chemistry |
| Brand names | Hinged Arms; Babyroo TN300; DRAEGER JAUNDICE METER JM-105; Evita V800 Evita V600; Atlan A350; Atlan A350 XL; Atlan A100 XL; Atlan A100 |
| First new listing | 2026-05-15 |
| Latest new listing | 2026-08-06 |
| FDA registration number | 9611500 |
| Registration expires | 2027-12-31 |
| amount percentile | 87th of 2,570 (median 1, 5.0x median) |
| Peer records CSV (37 DE records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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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: 2026-08-06
- 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: Draegerwerk AG & Co. KGaA and 37 Delaware peers
- Delaware DeviceEstablishmentPulse records like this one: 37
- Draegerwerk AG & Co. KGaA's amount: 87th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Delaware peer: $7,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
75 / 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.
What is the DeviceEstablishmentPulse record for Draegerwerk AG & Co. KGaA in LUEBECK Schleswig-Holstein, Delaware?
Draegerwerk AG & Co. KGaA (LUEBECK Schleswig-Holstein, DE), a manufacturer, added 5 FDA device listings between 2026-05-15 and 2026-08-06.
How does Draegerwerk AG & Co. KGaA compare to other Delaware DeviceEstablishmentPulse records?
Its amount of 5 sits in the upper half (87th percentile) of 2,570 records; the median is 1. It is 90 days old; check the official source for later updates before acting. Its Score of 75/100 puts it among the stronger signals in this feed.
Draegerwerk AG & Co. KGaA vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Draegerwerk AG & Co. KGaA | LUEBECK Schleswig-Holstein, DE | 5 | 87th | 2026-08-06 |
| Inquis Medical, Inc. | Menlo Park, CA | 5 | 87th | 2026-10-16 |
| Boston Scientific Corp., Marina Bay Cust. Fulfillment Center | Quincy, MA | 6 | 88th | 2026-10-16 |
| Piraeus Medical, Inc. | Maple Grove, MN | 4 | 83rd | 2026-10-12 |
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DeviceEstablishmentPulse: Manufacturer DeviceEstablishmentPulse: Foreign establishment DeviceEstablishmentPulse: records in Delaware
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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.