CRESEN INC

FDA Device Registration & Listing · Pleasanton, CA, US · Registration 3030176940

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
3030176940
FEI Number
3030176940
Entity Name
CRESEN INC
City/State/Country
Pleasanton, CA, US
Establishment Address
6200 Stoneridge Mall Rd Fl 3, Pleasanton, CA 94588, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
CRESEN Inc (Owner Number: 10089823)
Owner / Operator Contact Address
6200 Stoneridge Mall Rd Fl 3, Pleasanton, CA 94588, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K252211
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2025-12-31

Official Correspondent

Namheon Lee

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CRESEN 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
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030176940. Last updated year: 2026. Please use registration number 3030176940 when referencing this establishment in official correspondence.
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