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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 12 of 17

Device	Model / Reference	Registries	Class	Status
Reprocessed 300 Sagittal Saw Blade	AR-300-045S	FDA UDI	Class I	Active
Reprocessed Reflex Ultra 65 PlasmaWand	EIC4865-01	FDA UDI	Class II	Active
Reprocessed Small Bone Osc Sagittal Blade, 11.5 x 9.0 x 0.38mm	KM3-411	FDA UDI	Class I	Active
Reprocessed 5.0mm Ultra-Aggressive Blade Plus	283729	FDA UDI	Class I	Active
Reprocessed 2.9mm Gator Blade, 7.6cm, Large Hub	C9961A	FDA UDI	Class I	Active
Reprocessed 4.0mm Cool Cut Oval Bur, 8 Flute	AR-8400OBE	FDA UDI	Class I	Active
Reprocessed 2.3mm Bevel Arthrowand, 35 deg, Short	AC2823-01	FDA UDI	Class II	Active
Reprocessed Colorado Microdissect Needle, 2.35 x 40mm	N104A	FDA UDI	Class II	Active
Reprocessed 4mm Diamond Coated Bur	S-4D	FDA UDI	Class I	Active
Reprocessed 2.9mm Skimmer Angle Tip Blade, 18cm	18-82925HR	FDA UDI	Class I	Active
Reprocessed Dual Cut Sagittal Blade, 18 x 90 x 1.35mm	4118-135-090	FDA UDI	Class I	Active
Reprocessed 1.5mm Drill Bit, Quick Coupling, 85mm	310.15	FDA UDI	Class I	Active
Reprocessed Twist-in Cannula w/Obturator, 8.25mm x 7cm	AR-6530	FDA UDI	Class I	Active
Reprocessed 3.0mm Hooded Abrasion Bur	375-647-000	FDA UDI	Class I	Active
Reprocessed 4.0mm Angled Aggressive Serrated Blade, 40 Deg	5290-440-100	FDA UDI	Class I	Active
Reprocessed TAC-C II Probe	7209628ST	FDA UDI	Class II	Active
Reprocessed 300 Sagittal Saw Blade	AR-300-043S	FDA UDI	Class I	Active
Reprocessed Arthroscopic 2.0mm Drill	MS-DCR20	FDA UDI	Class I	Active
Reprocessed 4.3mm Quadcut Blade	18-84380HR	FDA UDI	Class I	Active
Reprocessed 2.8mm Surgibit Drill, 5"	MS-DC28	FDA UDI	Class I	Active
Reprocessed Oscillating Saw Blade, 19.5 x 71 x 1.2mm	5071-553	FDA UDI	Class I	Active
Reprocessed 2.3mm VAPR Wedge Electrode	227203	FDA UDI	Class II	Active
Reprocessed MicroNeedle 3cm	138505-10	FDA UDI	Class II	Active
Reprocessed 5.5mm Cool Cut Double Cut Blade	AR-8550DC	FDA UDI	Class I	Active
Reprocessed Dual Cut Sagittal Blade, 25 x 100 x 1.27 mm	4125-127-100	FDA UDI	Class I	Active
Reprocessed 4.5mm Round Bur, High Speed	18-84560HS	FDA UDI	Class I	Active
Reprocessed 2.5mm Resurfacing Tool	1900-015-025	FDA UDI	Class I	Active
Reprocessed Procise Max Plasma Wand	EIC8898-01	FDA UDI	Class II	Active
Reprocessed Straightshot to XPS	18-95522	FDA UDI	Class I	Active
Reprocessed Sagittal Saw Blade, 90 x 25 x 1.27mm	6125-127-100	FDA UDI	Class I	Active
Reprocessed 2mm Diamond Ball, Extended Length	S-2D-G1	FDA UDI	Class I	Active
Reprocessed 2.8mm Standard Jacobs Twist Drill	8054-013	FDA UDI	Class I	Active
Reprocessed 3.5m Tricut Blade, Rotatable	18-83504HRT	FDA UDI	Class I	Active
Reprocessed 2.9mm Full Radius Blade	3419	FDA UDI	Class I	Active
Reprocessed Sagittal Saw Blade, 18.6 x 1.24 x 84.4mm	2108-182	FDA UDI	Class I	Active
Reprocessed Driver Hex, Sterilemica, Screw System, 2.0mm	57S02020	FDA UDI	Class I	Active
Reprocessed 2.9mm Inferior Turbinate Blade, Rotatable	18-82940HR	FDA UDI	Class I	Active
Reprocessed Mica Drill Bit, 2.2mm	57S00022	FDA UDI	Class I	Active
Reprocessed 2.7mm Drill Bit, 100mm	310.26	FDA UDI	Class I	Active
Reprocessed 3.5mm Great White Blade	9399A	FDA UDI	Class I	Active
Reprocessed 2.9mm Skimmer Angle Tip Blade, 18cm	18-82925T	FDA UDI	Class I	Active
Reprocessed 3mm Round Fine Diamond ENT Bur, Fine	31133069	FDA UDI	Class I	Active
Reprocessed 2.5mm Curved Diamond DCR Bur	18-82569HS	FDA UDI	Class I	Active
Reprocessed Aggressive Medium Blade, 31 x 9 mm	2296-3-525	FDA UDI	Class I	Active
Reprocessed 4.2mm Bone Cutter, HL, 19cm	AR-6420BC	FDA UDI	Class I	Active
Reprocessed Micro Choice Sagittal Blade, Fine, 4.5 x 25.5mm	5023-139	FDA UDI	Class I	Active
Reprocessed 5mm Endoshears, 33cm, Monopolar	176643	FDA UDI	Class II	Active
Reprocessed Long Narrow Blade, 29.5 x 7 mm	2296-3-115	FDA UDI	Class I	Active
Reprocessed Celon ProSleep Plus RFITT, 1.3mm, 0-25W, 2 Pins.	WB990311	FDA UDI	Class II	Active
Reprocessed 5.5mm Cannula/Obturator, Conical Tip, No Holes	7204895	FDA UDI	Class I	Active

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