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

Guangzhou Wondfo Biotech Co., Ltd. (Dongguan Guangdong): 11 new FDA device listings, incl. test, propoxyphene, over the counter. Its amount of 11 is top-decile (94th percentile of 2,570 records). Dated 128 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: 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: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentGuangzhou Wondfo Biotech Co., Ltd.
RoleManufacturer
Establishment typesManufacture Medical Device
LocationDongguan Guangdong, CN
New listings11
DevicesTest, Propoxyphene, Over The Counter; Test, Amphetamine, Over The Counter; Test, Opiates, Over The Counter; Enzyme Immunoassay, Phencyclidine; Test, Cannabinoid, Over The Counter; Test, Barbiturate, Over The Counter; Test, Methamphetamine, Over The Counter; Test, Cocaine And Cocaine Metabolites, Over The Counter; Test, Benzodiazepine, Over The Counter; Test, Tricyclic Antidepressants, Over The Counter
Product codesQBF, NFT, NGL, LCM, NFW, PTH, NGG, NFY, NFV, QAW, PTG
Device classesClass II, Unclassified
Medical specialtiesClinical Toxicology
Brand namesSAFElife™ T-Dip Multi-Drug Urine Test Panel Dx; PRIME SCREEN® Single Panel Urine Test Cannabinoids (THC20)
First new listing2026-06-29
Latest new listing2026-06-29
FDA registration number3023322455
Registration expires2027-12-31
amount percentile94th of 2,570 (median 1, 11.0x 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: 2026-10-28
  • 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: Guangzhou Wondfo Biotech Co., Ltd. and 687 CN peers

  • CN DeviceEstablishmentPulse records like this one: 687
  • Guangzhou Wondfo Biotech Co., Ltd.'s amount: 94th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every CN peer: $137,400 (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 Dongguan Guangdong?

Guangzhou Wondfo Biotech Co., Ltd. (Dongguan 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 11.0x the median of 1 across 2,570 records. It is 128 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.Dongguan Guangdong, CN1194th2026-06-29
Boston Scientific CorporationCoventry, RI1093rd2026-10-16
Paragon 28Englewood, CO992nd2026-10-08
Surgentec LLCBoca Raton, FL1596th2026-10-16

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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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