Respironics Inc. (specification developer, Murrysville, PA): 1 new FDA device listing, incl. ventilator, non-continuous (respirator)

Respironics Inc. (Murrysville, Pennsylvania): 1 new FDA device listing, incl. ventilator, non-continuous (respirator). Its amount of 1 is above the median of 1 (50th percentile). Dated 37 days ago, it serves as a historical benchmark. Score 80/100. 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: 1 · 50th percentile of 2,570 DeviceEstablishmentPulse records · 1.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 43 related PA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentRespironics Inc.
Owner / operatorPhilips Medical Systems International BV
RoleSpecification developer (outsources manufacturing)
Establishment typesComplaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility
LocationMurrysville, PA, US
New listings1
DevicesVentilator, Non-Continuous (Respirator)
Product codesBZD
Device classesClass II
Medical specialtiesAnesthesiology
Brand namesAltis Full Face Mask
First new listing2026-09-29
Latest new listing2026-09-29
FDA registration number2518422
Registration expires2026-12-31
amount percentile50th of 2,570 (median 1, 1.0x 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: 2026-09-29
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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Top DeviceEstablishmentPulse records (PA first): Philips Ultrasound LLC (contract manufacturer, Reedsville, P · Arch Medical Solutions - Philadelphia, LLC Dba Jade Precisio · Globus Medical, Inc. (manufacturer, Audubon, PA) · Alta Smiles, LLC (manufacturer, Fort Washington, PA) · Synthes (USA) Products LLC (specification developer, West Ch · 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: Respironics Inc. and 44 Pennsylvania peers

  • Pennsylvania DeviceEstablishmentPulse records like this one: 44
  • Respironics Inc.'s amount: 50th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Pennsylvania peer: $8,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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80 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • U.S. establishment.
  • Listed in the last 45 days.

What is the DeviceEstablishmentPulse record for Respironics Inc. in Murrysville, Pennsylvania?

Respironics Inc. (Murrysville, PA), a specification developer (outsources manufacturing), added 1 FDA device listing on 2026-09-29.

How does Respironics Inc. compare to other Pennsylvania DeviceEstablishmentPulse records?

Its amount of 1 sits in the upper half (50th percentile) of 2,570 records; the median is 1. It is 37 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.

Respironics Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Respironics Inc.Murrysville, PA150th2026-09-29
Davol Inc., Sub. C.R. Bard, Inc.Warwick, RI377th2026-10-14
Ge Medical Systems, LLCWaukesha, WI377th2026-10-06
Align Technology, Inc.San Jose, CA377th2026-09-30

Related records

DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Pennsylvania

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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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