DeviceEstablishmentPulse / report
Cardinal Health 200, LLC (other, Waukegan, IL): 8 new FDA device listings, incl. fentanyl and other opioid protection glove
Cardinal Health 200, LLC (Waukegan, Illinois): 8 new FDA device listings, incl. fentanyl and other opioid protection glove. Its amount of 8 is top-decile (91st percentile of 2,570 records). Dated 22 days ago, it is in the active follow-up window. 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: 8 · 91th percentile of 2,570 DeviceEstablishmentPulse records · 8.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 94 related IL DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Cardinal Health 200, LLC |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Waukegan, IL, US |
| New listings | 8 |
| Devices | Fentanyl And Other Opioid Protection Glove; Polymer Patient Examination Glove; Medical Glove, Specialty; Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs; Dressing, Wound, Drug; Depressor, Tongue, Non-Surgical; Catheter, Retention Type, Balloon; Gown, Surgical |
| Product codes | QDO, LZA, LZC, OPJ, FRO, FMA, EZL, FYA |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | General Hospital, Gastroenterology, Urology, General, Plastic Surgery |
| Brand names | Stainless Steel Tongue Cleaner |
| First new listing | 2026-06-12 |
| Latest new listing | 2026-10-13 |
| FDA registration number | 1423537 |
| Registration expires | 2027-12-31 |
| amount percentile | 91th of 2,570 (median 1, 8.0x median) |
| Peer records CSV (95 IL 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: 2026-10-13
- 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: Cardinal Health 200, LLC and 95 Illinois peers
- Illinois DeviceEstablishmentPulse records like this one: 95
- Cardinal Health 200, LLC's amount: 91st percentile of 2,570 records
- Timing: Medium: dated in the last 30 days
- Estimated pipeline if you contact every Illinois peer: $19,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
75 / 100 Score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
- Listed in the last 45 days.
What is the DeviceEstablishmentPulse record for Cardinal Health 200, LLC in Waukegan, Illinois?
Cardinal Health 200, LLC (Waukegan, IL), a other, added 8 FDA device listings between 2026-06-12 and 2026-10-13.
How does Cardinal Health 200, LLC compare to other Illinois DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 8 is 8.0x the median of 1 across 2,570 records. It is 22 days old, still within a typical 45-day follow-up window. Its Score of 75/100 puts it among the stronger signals in this feed.
Cardinal Health 200, LLC vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Cardinal Health 200, LLC | Waukegan, IL | 8 | 91st | 2026-10-13 |
| Advance-Esthetic LLC | Fort Lauderdale, FL | 8 | 91st | 2026-10-12 |
| Metier Medical (USA) LLC | Ponte Vedra Beach, FL | 7 | 90th | 2026-10-16 |
| Shenb America, Inc. | Brea, CA | 10 | 93rd | 2026-08-21 |
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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.