Saint-Gobain Life Sciences (Hangzhou) Co., Ltd (contract manufacturer, Hangzhou Zhejiang, CN): 27 new FDA device listings, incl. accessories, cleaning, for endoscope

Saint-Gobain Life Sciences (Hangzhou) Co., Ltd (Hangzhou Zhejiang): 27 new FDA device listings, incl. accessories, cleaning, for endoscope. Its amount of 27 is top-decile (98th percentile of 2,709 records). Dated 100 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: 27 · 98th percentile of 2,709 DeviceEstablishmentPulse records · 13.5x the median

Free preview: all 14 published fields of this record are shown below. Locked: 499 related CN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentSaint-Gobain Life Sciences (Hangzhou) Co., Ltd
Owner / operatorSaint-Gobain Life Sciences (Hangzhou) Co., Ltd.
RoleContract manufacturer
Establishment typesManufacture Medical Device for Another Party (Contract Manufacturer)
LocationHangzhou Zhejiang, CN
New listings27
DevicesAccessories, Cleaning, For Endoscope; Sterilant, Medical Devices; Accessories, Germicide, Cleaning, For Endoscopes; Circuit, Breathing (W Connector, Adaptor, Y Piece)
Product codesFEB, MED, NZA, CAI
Device classesClass I, Class II
Medical specialtiesGastroenterology, Urology, General Hospital, Anesthesiology
First new listing2026-07-22
Latest new listing2026-07-28
FDA registration number3008157119
Registration expires2026-12-31
amount percentile98th of 2,709 (median 2, 13.5x 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: 2026-07-28
  • 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: Saint-Gobain Life Sciences (Hangzhou) Co., Ltd and 720 CN peers

  • CN DeviceEstablishmentPulse records like this one: 720
  • Saint-Gobain Life Sciences (Hangzhou) Co., Ltd's amount: 98th percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every CN peer: $144,000 (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 Saint-Gobain Life Sciences (Hangzhou) Co., Ltd in Hangzhou Zhejiang?

Saint-Gobain Life Sciences (Hangzhou) Co., Ltd (Hangzhou Zhejiang, CN), a contract manufacturer, added 27 FDA device listings between 2026-07-22 and 2026-07-28.

How does Saint-Gobain Life Sciences (Hangzhou) Co., Ltd compare to other DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 27 is 13.5x the median of 2 across 2,709 records. It is 100 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.

Saint-Gobain Life Sciences (Hangzhou) Co., Ltd vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Saint-Gobain Life Sciences (Hangzhou) Co., LtdHangzhou Zhejiang, CN2798th2026-07-28
Zimmer, Inc.Warsaw, IN2898th2026-09-29
Millstone Medical Outsourcing LLC.Fall River, MA2497th2026-10-08
Philips Ultrasound LLCReedsville, PA3298th2026-09-30

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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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