DeviceEstablishmentPulse / report
Wondfo USA Co., Ltd. (other, Bolingbrook, IL): 11 new FDA device listings, incl. enzyme immunoassay, phencyclidine
Wondfo USA Co., Ltd. (Bolingbrook, Illinois): 11 new FDA device listings, incl. enzyme immunoassay, phencyclidine. Its amount of 11 is top-decile (94th percentile of 2,570 records). Dated 91 days ago, it serves as a historical benchmark. Score 65/100. 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: 11 · 94th percentile of 2,570 DeviceEstablishmentPulse records · 11.0x 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 | Wondfo USA Co., Ltd. |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Bolingbrook, IL, US |
| New listings | 11 |
| Devices | Enzyme Immunoassay, Phencyclidine; Test, Opiates, Over The Counter; Test, Barbiturate, Over The Counter; Test, Cannabinoid, Over The Counter; Test, Methadone, Over The Counter; Test, Cocaine And Cocaine Metabolites, Over The Counter; Test, Methamphetamine, Over The Counter; Test, Benzodiazepine, Over The Counter; Test, Propoxyphene, Over The Counter; Test, Tricyclic Antidepressants, Over The Counter |
| Product codes | LCM, NGL, PTH, NFW, PTG, NFY, NGG, NFV, QBF, QAW, NFT |
| Device classes | Class II, Unclassified |
| Medical specialties | Clinical Toxicology |
| Brand names | SAFElife T-Dip Multi-Drug Urine Test Panel Dx; PRIME SCREEN® Single Panel Urine Test Cannabinoids (THC20) |
| First new listing | 2026-08-05 |
| Latest new listing | 2026-08-05 |
| FDA registration number | 3007606081 |
| Registration expires | 2027-12-31 |
| amount percentile | 94th of 2,570 (median 1, 11.0x 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: 2026-08-05
- 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: Wondfo USA Co., Ltd. and 95 Illinois peers
- Illinois DeviceEstablishmentPulse records like this one: 95
- Wondfo USA Co., Ltd.'s amount: 94th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Illinois peer: $19,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
65 / 100 Score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Wondfo USA Co., Ltd. in Bolingbrook, Illinois?
Wondfo USA Co., Ltd. (Bolingbrook, IL), a other, added 11 FDA device listings on 2026-08-05.
How does Wondfo USA Co., Ltd. compare to other Illinois DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 11 is 11.0x the median of 1 across 2,570 records. It is 91 days old; check the official source for later updates before acting.
Wondfo USA Co., Ltd. vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Wondfo USA Co., Ltd. | Bolingbrook, IL | 11 | 94th | 2026-08-05 |
| Premium Plus Dental Supplies Inc | Brooklyn, NY | 12 | 95th | 2026-09-25 |
| Cardinal Health 200, LLC | Waukegan, IL | 8 | 91st | 2026-10-13 |
| Advance-Esthetic LLC | Fort Lauderdale, FL | 8 | 91st | 2026-10-12 |
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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.