Aps Materials Inc. Ireland (contract manufacturer, Waterford Waterford(County), IE): 8 new FDA device listings, incl. prosthesis, shoulder, semi-constrained, metal/polymer + additive, ceme

Aps Materials Inc. Ireland (Waterford Waterford(County)): 8 new FDA device listings, incl. prosthesis, shoulder, semi-constrained, metal/polymer + additive, ceme. Its amount of 8 is top-decile (90th percentile of 2,709 records). Dated 150 days ago, it serves as a historical benchmark. Score 70/100. 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: 8 · 90th percentile of 2,709 DeviceEstablishmentPulse records · 4.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 20 related IE DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentAps Materials Inc. Ireland
Owner / operatorAPS Materials Inc. Ireland
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationWaterford Waterford(County), IE
New listings8
DevicesProsthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented; Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented; Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented; Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented; Shoulder Prosthesis, Reverse Configuration; Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Product codesPAO, KWT, HSD, MBF, PHX, KWS
Device classesClass II
Medical specialtiesOrthopedic
Brand namesComprehensive Reverse Shoulder System; Comprehensive Reverse Shoulder - HA Glenosphere Baseplates
First new listing2026-05-20
Latest new listing2026-06-08
FDA registration number3007740680
Registration expires2026-12-31
amount percentile90th of 2,709 (median 2, 4.0x 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: 2026-06-08
  • 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: Aps Materials Inc. Ireland and 21 IE peers

  • IE DeviceEstablishmentPulse records like this one: 21
  • Aps Materials Inc. Ireland's amount: 90th percentile of 2,709 records
  • Timing: Low: older than 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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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 Aps Materials Inc. Ireland in Waterford Waterford(County)?

Aps Materials Inc. Ireland (Waterford Waterford(County), IE), a contract manufacturer, added 8 FDA device listings between 2026-05-20 and 2026-06-08.

How does Aps Materials Inc. Ireland compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 8 is 4.0x the median of 2 across 2,709 records. It is 150 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.

Aps Materials Inc. Ireland vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Aps Materials Inc. IrelandWaterford Waterford(County), IE890th2026-06-08
Biopro, Inc.Port Huron, MI1092nd2026-10-15
NGInstruments, Inc dba Avalign Cutting InstrumentsWarsaw, IN483rd2026-10-16
Cook Medical LLCBloomington, IN483rd2026-10-13

Related records

DeviceEstablishmentPulse: Contract manufacturer DeviceEstablishmentPulse: Foreign establishment

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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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