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SCANLAN INTERNATIONAL INC

United States·US-MF-000010251

Last updated May 25, 2026

What SCANLAN INTERNATIONAL INC makes

SCANLAN International Inc manufactures surgical instruments designed for neurosurgery and vascular procedures, including needle holders, forceps, clamps, scissors, and vascular appliers. Their portfolio includes micro-forceps, temporary clipping tools, and specialized cutting instruments like the Kerrison Punch, tailored for precision in delicate surgical applications.

The company’s devices are classified under Class I in the EU regulatory framework and are listed in the eudamed database. SCANLAN International Inc 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 types of medical devices does SCANLAN International Inc manufacture?

SCANLAN International Inc specializes in surgical instruments used primarily in neurosurgery and vascular procedures. Their product line includes needle holders, forceps, clamps, scissors, vascular appliers, and specialized tools like the Kerrison Punch. These instruments are designed for precision in delicate surgical applications, such as micro-forceps for fine tissue manipulation or temporary clipping tools for vascular control.

Where is SCANLAN International Inc based?

SCANLAN International Inc is headquartered in the United States. The company’s location in the US influences its regulatory compliance framework, though individual devices must meet specific authorization requirements in each market where they are sold.

Which regulatory registries list SCANLAN International Inc’s devices?

SCANLAN International Inc’s devices are listed in the eudamed database, which is the European Union’s central registry for medical devices. This listing is required for transparency and traceability under EU regulations, particularly for Class I devices, which are subject to mandatory registration in eudamed.

How are SCANLAN International Inc’s devices classified under EU regulations?

SCANLAN International Inc’s devices fall under Class I classification in the EU regulatory framework. This classification applies to low-risk surgical instruments like needle holders, forceps, and scissors, which generally require less stringent pre-market evaluation compared to higher-risk devices. However, compliance with essential requirements and regulatory obligations (such as labeling and traceability) remains mandatory.

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

Information

Country
United States
Address
One, Scanlan Plaza, Saint Paul, United States
LinkedIn
—
Facebook
—
Phone
+1 651-298-0997
PRRC Contact
Waylon Vanderpoel
EUDAMED SRN
US-MF-000010251
FDA FEI Number
—
DUNS Number
023055619

Catalogue (2865)

Page 5 of 58
DeviceModel / ReferenceRegistriesClassStatus
SCANLAN® Yasargil‑Type Temporary Clip 3786-28N
EUDAMED
Class IActive
SCANLAN® Richards Micro Needle Holder 3003-452N
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-220PF
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-20E
EUDAMED
Class IActive
SCANLAN® Russian Forceps Q2434-4
EUDAMED
Class IActive
SCANLAN® Adson‑Brown Tissue Forceps 4004-30N
EUDAMED
Class IActive
SCANLAN® Baby Vascular Clamp Q2350-2
EUDAMED
Class IActive
SCANLAN® Phlebectomy Haemostat 5005-80N
EUDAMED
Class IActive
SCANLAN® Leriche Forceps 3003-14
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-217N
EUDAMED
Class IActive
SCANLAN® Jewelers Forceps 4004-07N
EUDAMED
Class IActive
SCANLAN® Micro Forceps 4004-250N
EUDAMED
Class IActive
SCANLAN® Crile Forceps 4118-05
EUDAMED
Class IActive
SCANLAN® Universal Suction Handle 9009-930N
EUDAMED
Class IActive
SCANLAN® CardioVasive™ /Thoracoscopic Duval Clamp 9909-204-1
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-816N
EUDAMED
Class IActive
SCANLAN® SUNDT™ Graduated Suction System 9009-940N
EUDAMED
Class IActive
SCANLAN® Micro Forceps 4004-260ST
EUDAMED
Class IActive
SCANLAN® Metzenbaum Scissors 7007-218-3SCN
EUDAMED
Class IActive
SCANLAN® SuperCut™ rongeur 8008-700
EUDAMED
Class IActive
SCANLAN® CardioVasive™ /Thoracoscopic Fine Needle Holder 9009-648-12-1
EUDAMED
Class IActive
SCANLAN® Custom Aorta Clamp Q27052-2
EUDAMED
Class IActive
SCANLAN® Grasping Forceps 4910-34
EUDAMED
Class IActive
SCANLAN® Yasargil‑Type Temporary Clip Q25024-8
EUDAMED
Class IActive
SCANLAN® Crile Forceps 4111-05
EUDAMED
Class IActive
SCANLAN® Metzenbaum Scissors 7007-217SCN
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-20N
EUDAMED
Class IActive
SCANLAN® Thoracoscopic Dennis Dissector Q28132-9
EUDAMED
Class IActive
SCANLAN® CardioVasive™ DeBakey Clamp 9909-232-27B
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 4004-246T
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 3003-760T
EUDAMED
Class IActive
SCANLAN® Premier™ round spring style handle 7007-594N
EUDAMED
Class IActive
SCANLAN® Micro Forceps 4004-260T
EUDAMED
Class IActive
SCANLAN® Upper Kidney Transplant Clamp Q2577-2
EUDAMED
Class IActive
SCANLAN® Thumb Dressing Forceps 3000-12
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 3003-752N
EUDAMED
Class IActive
SCANLAN® Thorek‑Brown Tissue Forceps 1001-33
EUDAMED
Class IActive
SCANLAN® Baby Vascular Clamp 2002-235N
EUDAMED
Class IActive
SCANLAN® Super Cut™ Mayo Scissors Q2423-7
EUDAMED
Class IActive
SCANLAN® McGivney Hemorrhoidal Ligator 2813-01
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 3003-750N
EUDAMED
Class IActive
SCANLAN® Multi-Purpose DeBakey Clamp Q29010-2
EUDAMED
Class IActive
SCANLAN® CardioVasive™ DeBakey Cross Clamp 9909-200A
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 3003-714N
EUDAMED
Class IActive
SCANLAN® MacDougall Clamp Q29066-2
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-918N
EUDAMED
Class IActive
SCANLAN® Titanium Bulldog Clamp Q2525-2
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-906N
EUDAMED
Class IActive
SCANLAN® Thumb Dressing Forceps 3010-06
EUDAMED
Class IActive
SCANLAN® Thoracoscopic Forester Clamp 9909-223
EUDAMED
Class IActive

Related Companies

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Notified Bodies

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Scanlan International Inc. has one FDA recall record initiated on February 19, 2007, which is listed with a terminated status. The reason provided for the recall was that the product was incorrectly assembled by the manufacturer.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Feb 19, 2007Z-0701-2007—terminated

Incorrectly assembled by manufacturer