Creation Technologies

FDA Device Registration & Listing · Everett, WA, US · Registration 3004065885

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004065885
FEI Number
3004065885
Entity Name
Creation Technologies
City/State/Country
Everett, WA, US
Establishment Address
6300 Merrill Creek Pkwy, A100, Everett, WA 98203, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Creation Technologies (Owner Number: 10052600)
Owner / Operator Contact Address
6300 Merrill Creek Pkwy, A100, Everett, WA 98203, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GlideScope® BFlex™ 2 Regular 5 Single-Use Bronchoscope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EOQ Bronchoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4680 2024-12-02

Official Correspondent

Ryan Taylor

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Creation Technologies
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2126519 CREATION TECHNOLOGIES WISCONSIN INC. Oak Creek, WI, US
1000474105 CREATION TECHNOLOGIES Newark, NY, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K811059 Pentax Precision Instrument Corp. PENTAX BRONCHOFIBERSCOPE #FB-15A 1981-05-27
K142934 Covidien CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved 2015-06-17
K240075 FUJIFILM Healthcare Americas Corporation FUJIFILM Endoscope Model EB-710XT 2024-02-07

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0025-2020 AURIS HEALTH INC 2
Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004065885. Last updated year: 2026. Please use registration number 3004065885 when referencing this establishment in official correspondence.
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