CANNUFLOW, INC.

FDA Device Registration & Listing · Scotts Valley, CA, US · Registration 3004957622

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
3004957622
FEI Number
3004957622
Entity Name
CANNUFLOW, INC.
City/State/Country
Scotts Valley, CA, US
Establishment Address
1800 Green Hills Rd #105A, Scotts Valley, CA 95066, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
CANNUFLOW, INC. (Owner Number: 9068421)
Owner / Operator Contact Address
1800 Green Hills Rd #105A, --, Scotts Valley, CA 95066, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

DRYVIEW SCOPE SHIELD SportPort Talarus Small Joint Cannula DryVu Fluid Shield EntreVu Cannulated Obturator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NBH Accessories, Arthroscopic Orthopedic Class 1 888.1100 2004-11-18
GEA Cannula, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2024-01-25

Official Correspondent

THEODORE KUCKLICK

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K863293 Lifestream Int'L, Inc. DISPOSABLE SUCTION CANNULA NO. 902008-000 1986-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0040-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 3mm Offset (Blue) Catalog Number: 72201713 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0041-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 4mm Offset (Purple Catalog Number: 72201714 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0042-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 5mm Offset (Red) Catalog Number: 72201715 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0043-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 6mm Offset (Green) Catalog Number: 72201716 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0044-2011 Smith & Nephew, Inc. Endoscopy Division 1
Smith & Nephew Aimer Endofemoral 7mm Offset (Gold) Catalog Number: 72201717 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004957622. Last updated year: 2026. Please use registration number 3004957622 when referencing this establishment in official correspondence.
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