Takumi Precision Engineering Ltd (contract manufacturer, Limerick Limerick(County), IE): 10 new FDA device listings, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol

Takumi Precision Engineering Ltd (Limerick Limerick(County)): 10 new FDA device listings, incl. prosthesis, knee, patellofemorotibial, semi-constrained, cemented, pol. Its amount of 10 is top-decile (92nd percentile of 2,709 records). Dated 17 days ago, it is in the active follow-up window. Score 80/100. 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: 10 · 92th percentile of 2,709 DeviceEstablishmentPulse records · 5.0x the median

Free preview: all 13 published fields of this record are shown below. Locked: 20 related IE DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentTakumi Precision Engineering Ltd
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationLimerick Limerick(County), IE
New listings10
DevicesProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer; Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer; Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer; Prosthesis, Knee Patellofemorotibial, Partial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Product codesJWH, KRR, HSX, HRY, NPJ, LPH, JDI
Device classesClass II
Medical specialtiesOrthopedic
First new listing2026-10-19
Latest new listing2026-10-19
FDA registration number3007189546
Registration expires2027-12-31
amount percentile92th of 2,709 (median 2, 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: 2026-10-19
  • 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: Takumi Precision Engineering Ltd and 21 IE peers

  • IE DeviceEstablishmentPulse records like this one: 21
  • Takumi Precision Engineering Ltd's amount: 92nd percentile of 2,709 records
  • Timing: Medium: dated in the last 30 days
  • Estimated pipeline if you contact every IE peer: $4,200 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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80 / 100 Score

  • Contract manufacturer or sterilizer adding work.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Takumi Precision Engineering Ltd in Limerick Limerick(County)?

Takumi Precision Engineering Ltd (Limerick Limerick(County), IE), a contract manufacturer, added 10 FDA device listings on 2026-10-19.

How does Takumi Precision Engineering Ltd compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 10 is 5.0x the median of 2 across 2,709 records. It is 17 days old, still within a typical 45-day follow-up window. Its Score of 80/100 puts it among the stronger signals in this feed.

Takumi Precision Engineering Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Takumi Precision Engineering LtdLimerick Limerick(County), IE1092nd2026-10-19
Biopro, Inc.Port Huron, MI1092nd2026-10-15
Karl Storz Endoscopy-America, Inc.Auburn, MA1595th2026-10-08
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16

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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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