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SURETEK MEDICAL

Last updated September 17, 2026

What SURETEK MEDICAL makes

Suretek Medical manufactures reprocessed and single-use surgical instruments and accessories for orthopedic and endoscopic procedures, including arthroscopic shaver system blades, fluted surgical drill bits, surgical power tool handpieces, endoscopic electrosurgical handpieces and electrodes (both bipolar and monopolar), orthopaedic burs, surgical saw blades (sagittal), and paranasal sinus irrigation catheters. Specific examples include reprocessed sagittal blades, drill bits, shaver blades, skimmer angle tip blades, VAPR electrodes, carpal tunnel release blades, and twist-in cannulas.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system. Suretek Medical is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does Suretek Medical manufacture?

Suretek Medical produces reprocessed and single-use surgical instruments and accessories for orthopedic and endoscopic procedures, including arthroscopic shaver blades, surgical drill bits, power tool handpieces, electrosurgical handpieces/electrodes, orthopedic burs, sagittal saw blades, and paranasal sinus irrigation catheters.

Where is Suretek Medical based?

Suretek Medical is based in the United States, as indicated by the country information provided in the device data.

Which regulatory registries list Suretek Medical's devices?

Suretek Medical's devices are listed in the FDA's Unique Device Identification (FDA UDI) system, as specified in the device data.

How are Suretek Medical's devices classified?

Suretek Medical's devices are classified as Class I and Class II medical devices, which represents their level of regulatory control based on their risk to patients and users.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: 25-B MAPLE CREEK CIRCLE, GREENVILLE, SC, 29607
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005575604
DUNS Number: 785616934

Catalogue (815)

Page 17 of 17

Device	Model / Reference	Registries	Class	Status
Reprocessed PassPort Button Cannula, 8mm x 2cm	AR-6592-08-20	FDA UDI	Class I	Active
Reprocessed Shaver Blade Straight 2.1mm Double Serrated	1601070	FDA UDI	Class I	Active
Reprocessed 5.5mm Barrel Bur, 12 Flute	375-951-012	FDA UDI	Class I	Active
Reprocessed VAPR Cool Pulse Electrode	228146	FDA UDI	Class II	Active
Reprocessed 3.0 CoolCut Dissector Blade	AR-9300DS	FDA UDI	Class I	Active
Reprocessed 2.5mm Dome 60 Arthrowand w/ Cable	AC3525-01	FDA UDI	Class II	Active
Reprocessed 7 mm, Badger Cannulated Drill Bit	C8582	FDA UDI	Class I	Active
Reprocessed 2.0mm Cannulated Drill Bit	03-4000-18	FDA UDI	Class I	Active
Reprocessed 2.3mm VAPR Side Effect Electrode, Short	227213ST	FDA UDI	Class II	Active
Reprocessed 3.0mm Round Stainless Steel Bur, Medium	03.000.010	FDA UDI	Class I	Active
Reprocessed 4mm High Speed Curved Cutting Bur, 15 Deg	18-84075HSE	FDA UDI	Class I	Active
Suretek Medical Reprocessed Electrosurgical Electrodes	K052692	FDA 510(k)	Class II	Active
Suretek Medical Reprocessed Arthroscopic Blades And Burs	K052695	FDA 510(k)	Class II	Active
Suretek Medical Reprocessed Compression Sleeves	K052691	FDA 510(k)	Class II	Active
Suretek Reprocessed Laparoscopic Instruments	K052690	FDA 510(k)	Class II	Active

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