Safetec Of America, Inc. (manufacturer, Buffalo, NY): 6 new FDA device listings, incl. accessories, cleaning brushes, for endoscope

Safetec Of America, Inc. (Buffalo, New York): 6 new FDA device listings, incl. accessories, cleaning brushes, for endoscope. Its amount of 6 is above the median of 2 (88th percentile). Dated 37 days ago, it serves as a historical benchmark. Score 95/100. 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: 6 · 88th percentile of 2,709 DeviceEstablishmentPulse records · 3.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 57 related NY DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentSafetec Of America, Inc.
Owner / operatorSafetec of America Inc
RoleManufacturer
Establishment typesRepack or Relabel Medical Device; Manufacture Medical Device
LocationBuffalo, NY, US
New listings6
DevicesAccessories, Cleaning Brushes, For Endoscope; Cement, Stomal Appliance, Ostomy; Urinary Drainage Collection Kit, For Indwelling Catheter; Scissors, Medical, Disposable; Catheter, Rectal For Continent Ileostomy; Brush, Cleaning, Tracheal Tube
Product codesMNL, EZR, FCN, JOK, KPH, EPE
Device classesClass I, Class II
Medical specialtiesGastroenterology, Urology, General Hospital, Anesthesiology
Brand namesUnited Contour Brush Endotracheal 9/16 in. x 16 in. package of 12; United Contour Brushes 1/4 in. x 16 in., package of 12; United Contour Brush Tracheal 9/16 in x 6 in., package of 1 set; United Contour Brush general cleaning set of 8; United Contour Brush set of 3, package of 1 set; United Contour Brush; United Contour Brush Tracheal 3/8 in. x 6 in. Package of 12; United Contour Brush Endotracheal set of 4, package of 1 set
First new listing2026-06-22
Latest new listing2026-09-29
FDA registration number1319744
Registration expires2026-12-31
amount percentile88th of 2,709 (median 2, 3.0x 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: 2026-11-04
  • 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: Safetec Of America, Inc. and 58 New York peers

  • New York DeviceEstablishmentPulse records like this one: 58
  • Safetec Of America, Inc.'s amount: 88th percentile of 2,709 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every New York peer: $11,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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95 / 100 Score

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

What is the DeviceEstablishmentPulse record for Safetec Of America, Inc. in Buffalo, New York?

Safetec Of America, Inc. (Buffalo, NY), a manufacturer, added 6 FDA device listings between 2026-06-22 and 2026-09-29.

How does Safetec Of America, Inc. compare to other New York DeviceEstablishmentPulse records?

Its amount of 6 sits in the upper half (88th percentile) of 2,709 records; the median is 2. It is 37 days old, still within a typical 45-day follow-up window. Its Score of 95/100 puts it among the stronger signals in this feed.

Safetec Of America, Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Safetec Of America, Inc.Buffalo, NY688th2026-09-29
Inter-Med, Inc.Racine, WI586th2026-10-22
Centerpoint Systems LLCWest Valley City, UT586th2026-10-21
GE Medical Systems Ultrasound and Primary Care Diagnostics, LLCWaukesha, WI586th2026-10-19

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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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