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T.A.G. Medical Products Corporation Ltd: FDA-registered device maker in Bar-Lev Northern, Israel, 1 510(k) clearance

Name: T.A.G. Medical Products Corporation Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

T.A.G. Medical Products Corporation Ltd is registered with the FDA (registration 3022132808) in Bar-Lev Northern, Israel. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 11, 2011. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3022132808
Address: Harotem 23, Bar-Lev Northern, Israel, 2015600
Owner or operator: TAG Medical products corporation LTD (9004870)
Roles: Contract manufacturer, Manufacturer
First device listed: May 22, 2016
Registered through: 2026
Brand names listed: 10 X 30 mm Flexible Cannula, 10 mm Flexible Cannula, 12 mm Flexible Cannula, 28MM SCREW, 28mm Screw & Top Hat, 30mm Screw & Top Hat, 32mm Screw & Top Hat, 34MM SCREW and more

Devices it lists

Device	Product code	Class	Role	Source
Cannula, Surgical, General & Plastic Surgery	GEA	1	Manufacturer	accessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment	HWE	1	Contract manufacturer	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Manufacturer	accessdata.fda.gov
Screw, Fixation, Bone	HWC	2	Manufacturer	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
April 11, 2011	K110763	LATARJET CORTICAL SCREW SET	HWC	Substantially Equivalent	T.A.G. Medical Products Corporation, Ltd.	accessdata.fda.gov

Compare with other makers

Updated April 11, 2011. 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.