Data / Medical devices / United States / Cell Surgical Network Corporation

Cell Surgical Network Corporation: FDA-registered device maker in Rancho Mirage, CA, United States, 1 510(k) clearance

Name: Cell Surgical Network Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Cell Surgical Network Corporation is registered with the FDA (registration 3016080683) in Rancho Mirage, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 7, 2012. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3016080683
Address: 72780 Country Club Drive Ste 301, Rancho Mirage, CA, United States, 92270
Owner or operator: Cell Surgical Network Corporation (10062017)
Roles: Repackager or relabeler
First device listed: August 22, 2023
Registered through: 2026
Brand names listed: SVF Kit, Smart Lock, TaraLock

Devices it lists

Device	Product code	Class	Role	Source
Apparatus, Suction, Operating-Room, Wall Vacuum Powered	GCX	2	Repackager or relabeler	accessdata.fda.gov
Instrument, Manual, Surgical, General Use	MDM	1	Repackager or relabeler	accessdata.fda.gov
System, Suction, Lipoplasty	MUU	2	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
December 7, 2012	K121703	LIPOKIT WITH DISPOSABLE 50CC AFT SYRINGE	MUU	Substantially Equivalent	Medi-Khan USA, Inc.	accessdata.fda.gov

Compare with other makers

Updated December 7, 2012. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.