Astron Medtech Co., Ltd. (repackager or relabeler, Taipei, TW): 5 new FDA device listings, incl. suture, nonabsorbable, synthetic, polyethylene

Astron Medtech Co., Ltd. (Taipei): 5 new FDA device listings, incl. suture, nonabsorbable, synthetic, polyethylene. Its amount of 5 is above the median of 1 (87th percentile). Dated 125 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: 5 · 87th percentile of 2,570 DeviceEstablishmentPulse records · 5.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 49 related TW DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentAstron Medtech Co., Ltd.
RoleRepackager or relabeler
Establishment typesForeign Private Label Distributor; Repack or Relabel Medical Device
LocationTaipei, TW
New listings5
DevicesSuture, Nonabsorbable, Synthetic, Polyethylene; Fastener, Fixation, Nondegradable, Soft Tissue; Accessories, Arthroscopic; Orthopedic Manual Surgical Instrument
Product codesGAT, MBI, NBH, LXH
Device classesClass I, Class II
Medical specialtiesGeneral, Plastic Surgery, Orthopedic
Brand namesTendMIN ® Suture Kit - Loop Suture; TendMIN ® Anchor Kit - Anchor; TendMIN ® Anchor Kit - Passer; TendMIN ® Suture Kit - Suture Tape; TendMIN ® Suture Kit - Grasper, Telescoping Needle
First new listing2026-06-26
Latest new listing2026-07-03
FDA registration number3044423486
Registration expires2026-12-31
amount percentile87th of 2,570 (median 1, 5.0x 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: 2026-07-03
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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Top DeviceEstablishmentPulse records (TW first): Zimmer Biomet Taiwan Co., Ltd. (foreign exporter, Taipei, TW · Syntec Scientific Corp. (contract manufacturer, CHANG HUA Ch · Miing Wei Co., Ltd. (contract manufacturer, Tsao-Twon Nantou · United Orthopedic Corp. (manufacturer, Kaohsiung, TW) · United Orthopedic Corporation (manufacturer, Hsinchu Hsinchu · Browse all by state and category →

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: Astron Medtech Co., Ltd. and 50 TW peers

  • TW DeviceEstablishmentPulse records like this one: 50
  • Astron Medtech Co., Ltd.'s amount: 87th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every TW peer: $10,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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55 / 100 Score

  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Astron Medtech Co., Ltd. in Taipei?

Astron Medtech Co., Ltd. (Taipei, TW), a repackager or relabeler, added 5 FDA device listings between 2026-06-26 and 2026-07-03.

How does Astron Medtech Co., Ltd. compare to other DeviceEstablishmentPulse records?

Its amount of 5 sits in the upper half (87th percentile) of 2,570 records; the median is 1. It is 125 days old; check the official source for later updates before acting.

Astron Medtech Co., Ltd. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Astron Medtech Co., Ltd.Taipei, TW587th2026-07-03
Tpc Advanced Technology, Inc.City Industry, CA483rd2026-09-28
Nam Ha Viet Nam Trading Company LimitedHanoi Ha Noi, VN377th2026-09-24
VIVE Health LLCNaples, FL1093rd2026-10-14

Related records

DeviceEstablishmentPulse: Repackager or relabeler DeviceEstablishmentPulse: Foreign establishment

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✓ Read-only, live public data · Key and unlock right after payment · Card, Apple Pay, Google Pay or Link via Stripe · Refunds on request within 14 days

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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