SSCOR, INC.

FDA Device Registration & Listing · Simi Valley, CA, US · Registration 2022724

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
2022724
FEI Number
2022724
Entity Name
SSCOR, INC.
City/State/Country
Simi Valley, CA, US
Establishment Address
2125 N. Madera Rd Unit C, Simi Valley, CA 93065, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SSCOR, Inc. (Owner Number: 10027309)
Owner / Operator Contact Address
2125 N. Madera Rd. Unit C, Simi Valley, CA 93065, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K964997
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
BTA Pump, Portable, Aspiration (Manual Or Powered) General, Plastic Surgery Class 2 878.4780 2008-10-23
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered General Hospital Class 2 880.6740 2008-10-23
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered General Hospital Class 2 880.6740 2009-10-09
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered General, Plastic Surgery Class 2 878.4780 2008-10-23
BTA Pump, Portable, Aspiration (Manual Or Powered) General, Plastic Surgery Class 2 878.4780 2008-10-23
BTA Pump, Portable, Aspiration (Manual Or Powered) General, Plastic Surgery Class 2 878.4780 2008-10-23
JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered General, Plastic Surgery Class 2 878.4780 2008-10-23
BTA Pump, Portable, Aspiration (Manual Or Powered) General, Plastic Surgery Class 2 878.4780 2008-10-23

Official Correspondent

Sam Say

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SSCOR, 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
K082762 Aardvark Medical AARDVARK NASAL IRRIGATION AND ASPIRATION DEVICE 2008-11-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0035-2007 Haemonetics Corporation 2
SmartSuction Harmony Powered Suction Device Model Number: HAR-E-115-US
Z-0038-05 Kinetic Concepts, Inc 2
V.A.C. X-Large Granufoam Dressing Part Numbers M6275065/5, V.A.C. ATS and V.A.C. Freedom and M6275043/5 V.A.C. Classic. Manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78230

Similar Registrations

Registration Number Establishment Name Location
3017435705 CENTESE, INC. Omaha, NE, US
2134752 AXCESOR LLC Menomonee Falls, WI, US
3010707607 KARL STORZ SE & CO. KG NEUHAUSEN OBECK Baden-Wurttemberg, DE
3010079067 MicroVention Costa Rica S.R.L. . Alajuela, CR
3005168196 PENUMBRA, INC. Alameda, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2022724. Last updated year: 2026. Please use registration number 2022724 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.