Data / Medical devices / Russia / Titan Surgical

Titan Surgical: FDA-registered device maker in KAZAN Tatarstan, Russia, 1 510(k) clearance

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

Titan Surgical is registered with the FDA (registration 9616972) in KAZAN Tatarstan, Russia. It lists 15 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 6, 1986. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 9616972
FEI number: 3006125446
Address: Bld. 109 Ul. Vosstaniya 100, Office 2, KAZAN Tatarstan, Russia, 420095
Owner or operator: TITAN SURGICAL (9039588)
Roles: Manufacturer, Repackager or relabeler, Specification developer
First device listed: November 12, 1999
Registered through: 2026
Brand names listed: Pilling, TITAN MEDICAL, TITANIUMEDICAL, TITANMEDICAL

Devices it lists

Device	Product code	Class	Role	Source
Caliper, Ophthalmic	HOE	1	Manufacturer	accessdata.fda.gov
Cannula, Ophthalmic	HMX	1	Manufacturer	accessdata.fda.gov
Clamp, Vascular	DXC	2	Manufacturer	accessdata.fda.gov
Forceps, General & Plastic Surgery	GEN	1	Manufacturer	accessdata.fda.gov
Forceps, Ophthalmic	HNR	1	Repackager or relabeler, Specification developer	accessdata.fda.gov
Holder, Needle, Gastroenterologic	FHQ	1	Manufacturer	accessdata.fda.gov
Hook, Ophthalmic	HNQ	1	Manufacturer	accessdata.fda.gov
Instrument, Manual, Surgical, General Use	MDM	1	Manufacturer	accessdata.fda.gov
Instruments, Surgical, Cardiovascular	DWS	1	Manufacturer	accessdata.fda.gov
Knife, Ophthalmic	HNN	1	Repackager or relabeler, Specification developer	accessdata.fda.gov
Needle, Ophthalmic Suturing	HNM	1	Repackager or relabeler, Specification developer	accessdata.fda.gov
Ring, Ophthalmic (Flieringa)	HNH	1	Manufacturer	accessdata.fda.gov
Scissors, Ophthalmic	HNF	1	Manufacturer	accessdata.fda.gov
Spatula, Ophthalmic	HND	1	Manufacturer	accessdata.fda.gov
Specula, Ophthalmic	HNC	1	Repackager or relabeler, Specification developer	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
June 6, 1986	K861924	MICRO ANASTOMOSIS CLAMP	DXC	Substantially Equivalent	Pilling Co.	accessdata.fda.gov

Compare with other makers

Updated June 6, 1986. 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.