Philips North America LLC (other, Cambridge, MA): 62 new FDA device listings, incl. analyzer, gas, sevoflurane, gaseous-phase (anesthetic concentration)

Philips North America LLC (Cambridge, Massachusetts): 62 new FDA device listings, incl. analyzer, gas, sevoflurane, gaseous-phase (anesthetic concentration). Its amount of 62 is top-decile (99th percentile of 2,709 records). Dated 167 days ago, it serves as a historical benchmark. Score 65/100. 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: 62 · 99th percentile of 2,709 DeviceEstablishmentPulse records · 31.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 72 related MA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentPhilips North America LLC
Owner / operatorPhilips Medical Systems International BV
RoleOther
Establishment typesComplaint File Establishment per 21 CFR 820.198
LocationCambridge, MA, US
New listings62
DevicesAnalyzer, Gas, Sevoflurane, Gaseous-Phase (Anesthetic Concentration); Monitor, St Segment With Alarm; Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm); Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms); Oximeter; Monitor, Breathing Frequency; Computer, Blood-Pressure; Calculator, Pulmonary Function Data; Computer, Diagnostic, Programmable; System, Network And Communication, Physiological Monitors
Product codesNHP, MLD, DRT, MHX, DQA, BZQ, DSK, BZC, DQK, MSX, FLL, DSJ, KOI, CBQ, GWQ
Device classesClass I, Class II
Medical specialtiesAnesthesiology, Cardiovascular, General Hospital, Neurology
Brand namesIntelliVue MX400, MX450, MX500, MX550, Rev. R; IntelliVue MX750/MX850,Flexible Module Server FMX-4, Rev. R; IntelliVue MX100, X3, MMX Rev. R; IntelliVue MMX Rev. R
First new listing2026-05-22
Latest new listing2026-05-22
FDA registration number3016618143
Registration expires2026-12-31
amount percentile99th of 2,709 (median 2, 31.0x 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: 2026-05-22
  • 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: Philips North America LLC and 73 Massachusetts peers

  • Massachusetts DeviceEstablishmentPulse records like this one: 73
  • Philips North America LLC's amount: 99th percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Massachusetts peer: $14,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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65 / 100 Score

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

What is the DeviceEstablishmentPulse record for Philips North America LLC in Cambridge, Massachusetts?

Philips North America LLC (Cambridge, MA), a other, added 62 FDA device listings on 2026-05-22.

How does Philips North America LLC compare to other Massachusetts DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 62 is 31.0x the median of 2 across 2,709 records. It is 167 days old; check the official source for later updates before acting.

Philips North America LLC vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Philips North America LLCCambridge, MA6299th2026-05-22
Karl Storz Endoscopy-America, Inc.El Segundo, CA1796th2026-10-19
Karl Storz Endoscopy-America, Inc.El Segundo, CA1595th2026-09-28
Premium Plus Dental Supplies IncBrooklyn, NY1395th2026-10-21

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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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