Cometech Vn Company Limited (contract manufacturer, Phu Thanh Ward Ho Chi Minh, VN): 7 new FDA device listings, incl. teeth, artificial, posterior with metal insert

Cometech Vn Company Limited (Phu Thanh Ward Ho Chi Minh): 7 new FDA device listings, incl. teeth, artificial, posterior with metal insert. Its amount of 7 is top-decile (90th percentile of 2,570 records). Dated 66 days ago, it serves as a historical benchmark. Score 70/100. 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: 39 related VN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentCometech Vn Company Limited
RoleContract manufacturer
Establishment typesRemanufacture Medical Device; Repack or Relabel Medical Device; Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
LocationPhu Thanh Ward Ho Chi Minh, VN
New listings7
DevicesTeeth, Artificial, Posterior With Metal Insert; Bracket, Metal, Orthodontic; Heat Source For Bleaching Teeth; Teeth, Preformed Gold Denture; Denture, Plastic, Teeth; Teeth, Artificial, Backing And Facing; Reliner, Denture, Over The Counter
Product codesELJ, EJF, EEG, ELN, ELM, ELK, EBP
Device classesClass I, Class II
Medical specialtiesDental
Brand namesCOMETECH VN
First new listing2026-08-31
Latest new listing2026-08-31
FDA registration number3048547325
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: 2026-08-31
  • 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: Cometech Vn Company Limited and 40 VN peers

  • VN DeviceEstablishmentPulse records like this one: 40
  • Cometech Vn Company Limited's amount: 90th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every VN peer: $8,000 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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70 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.

What is the DeviceEstablishmentPulse record for Cometech Vn Company Limited in Phu Thanh Ward Ho Chi Minh?

Cometech Vn Company Limited (Phu Thanh Ward Ho Chi Minh, VN), a contract manufacturer, added 7 FDA device listings on 2026-08-31.

How does Cometech Vn Company Limited 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 66 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.

Cometech Vn Company Limited vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Cometech Vn Company LimitedPhu Thanh Ward Ho Chi Minh, VN790th2026-08-31
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16
Cook Medical LLCBloomington, IN483rd2026-10-13
Swiss-American CDMO,LLCCarrollton, TX483rd2026-10-12

Related records

DeviceEstablishmentPulse: Contract manufacturer 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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