Hynaut Health Technology Co., LTD. (contract manufacturer, Qingdao Shandong, CN): 7 new FDA device listings, incl. catheter, infusion

Hynaut Health Technology Co., LTD. (Qingdao Shandong): 7 new FDA device listings, incl. catheter, infusion. Its amount of 7 is top-decile (90th percentile of 2,570 records). Dated 86 days ago, it serves as a historical benchmark. Score 55/100. 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: 7 · 90th percentile of 2,570 DeviceEstablishmentPulse records · 7.0x 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
EstablishmentHynaut Health Technology Co., LTD.
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer); Manufacture Medical Device
LocationQingdao Shandong, CN
New listings7
DevicesCatheter, Infusion; Needle, Suturing, Disposable; Needle, Aspiration And Injection, Disposable; Container, Specimen, Sterile; Container, Specimen, Urine, Drugs Of Abuse, Over The Counter; Applicator, Absorbent Tipped, Sterile; Container, Liquid Medication, Graduated
Product codesJCY, GAB, GAA, FMH, MPQ, KXG, KYW
Device classesClass I
Medical specialtiesGeneral, Plastic Surgery, Pathology, General Hospital
Brand namesIV CATHETER GUIDE - MACRODRIP PERFUSION SET V14; GUIA DE SUERO - PERFUS MACROGOTERO V14; AGUJA QUIRURGICA - TIPO DESCARTABLE - ESPECIFICACION 25/8 - UNIDAD VENTA C/U; AGUJA QUIRURGICA - TIPO DESCARTABLE - ESPECIFICACION 40/8 - UNIDAD VENTA C/U; SURGICAL NEEDLE - MEGHINI TYPE - SPECIFICATION 16G X 5"; Disposable needle 25/8 Terumo (21 G); Plastic Petri Dish 100 x 20 mm; Recipiente esteril descartable c/tapa rosca p/material biologico (recipiente esteril urocultivo)
First new listing2026-08-10
Latest new listing2026-08-10
FDA registration number3008808560
Registration expires2026-12-31
amount percentile90th of 2,570 (median 1, 7.0x 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: 2026-08-10
  • 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: Hynaut Health Technology Co., LTD. and 687 CN peers

  • CN DeviceEstablishmentPulse records like this one: 687
  • Hynaut Health Technology Co., LTD.'s amount: 90th 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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55 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Hynaut Health Technology Co., LTD. in Qingdao Shandong?

Hynaut Health Technology Co., LTD. (Qingdao Shandong, CN), a contract manufacturer, added 7 FDA device listings on 2026-08-10.

How does Hynaut Health Technology Co., LTD. compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 7 is 7.0x the median of 1 across 2,570 records. It is 86 days old; check the official source for later updates before acting.

Hynaut Health Technology Co., LTD. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Hynaut Health Technology Co., LTD.Qingdao Shandong, CN790th2026-08-10
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16
Cook Medical LLCBloomington, IN483rd2026-10-13
Swiss-American CDMO,LLCCarrollton, TX483rd2026-10-12

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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.

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