Guangzhou Wondfo Biotech Co., Ltd. (manufacturer, Guangzhou Guangdong, CN): 11 new FDA device listings, incl. test, propoxyphene, over the counter

Guangzhou Wondfo Biotech Co., Ltd. (Guangzhou Guangdong): 11 new FDA device listings, incl. test, propoxyphene, over the counter. Its amount of 11 is top-decile (93rd percentile of 2,709 records). Dated 129 days ago, it serves as a historical benchmark. Score 75/100. 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 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentGuangzhou Wondfo Biotech Co., Ltd.
RoleManufacturer
Establishment typesComplaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
LocationGuangzhou Guangdong, CN
New listings11
DevicesTest, Propoxyphene, Over The Counter; Test, Amphetamine, Over The Counter; Test, Opiates, Over The Counter; Enzyme Immunoassay, Phencyclidine; Test, Cocaine And Cocaine Metabolites, Over The Counter; Test, Methamphetamine, Over The Counter; Test, Cannabinoid, Over The Counter; Test, Barbiturate, Over The Counter; Test, Benzodiazepine, Over The Counter; Test, Tricyclic Antidepressants, Over The Counter
Product codesQBF, NFT, NGL, LCM, NFY, NGG, NFW, PTH, NFV, QAW, PTG
Device classesClass II, Unclassified
Medical specialtiesClinical Toxicology
Brand namesPRIME SCREEN® Single Panel Urine Test Cannabinoids (THC20); SAFElife™ T-Dip Multi-Drug Urine Test Panel Dx
First new listing2026-06-29
Latest new listing2026-06-29
FDA registration number3004635103
Registration expires2027-12-31
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: 2026-06-29
  • Data refreshed: 2026-11-04
  • 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, 04 Nov 2026 21:52:36 GMT

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Peer benchmark and outreach value: Guangzhou Wondfo Biotech Co., Ltd. and 720 CN peers

  • CN DeviceEstablishmentPulse records like this one: 720
  • Guangzhou Wondfo Biotech Co., Ltd.'s amount: 93rd percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every CN peer: $144,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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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 Guangzhou Wondfo Biotech Co., Ltd. in Guangzhou Guangdong?

Guangzhou Wondfo Biotech Co., Ltd. (Guangzhou Guangdong, CN), a manufacturer, added 11 FDA device listings on 2026-06-29.

How does Guangzhou Wondfo Biotech Co., Ltd. compare to other 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 129 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.

Guangzhou Wondfo Biotech Co., Ltd. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Guangzhou Wondfo Biotech Co., Ltd.Guangzhou Guangdong, CN1193rd2026-06-29
Biomerieux, Inc.Hazelwood, MO1294th2026-10-22
Boston Scientific CorporationCoventry, RI1092nd2026-10-16
Intuitive Surgical, Inc.Sunnyvale, CA1395th2026-10-22

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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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