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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 6 of 58
DeviceModel / ReferenceRegistriesClassStatus
SCANLAN® Titanium Micro Forceps 3003-922N
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-220N
EUDAMED
Class IActive
SCANLAN® Gerald DeBakey Forceps 4004-240N
EUDAMED
Class IActive
SCANLAN® Yasargil Micro Raspatory 3003-181N
EUDAMED
Class IActive
SCANLAN® Vannas Micro Scissors 3789-05N
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 4004-239N
EUDAMED
Class IActive
SCANLAN® Potts‑Smith Forceps 4004-110
EUDAMED
Class IActive
SCANLAN® Thoracoscopic Chitwood DeBakey Clamp Q29017-9
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 3003-750T
EUDAMED
Class IActive
SCANLAN® Rochester‑Pean Forceps 4140-08
EUDAMED
Class IActive
SCANLAN® Premier™ Jacobson Micro Scissors 7007-509N
EUDAMED
Class IActive
SCANLAN® Micro Forceps 4004-280T
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-782N
EUDAMED
Class IActive
SCANLAN® Ochsner Plaque Remover 9009-150N
EUDAMED
Class IActive
SCANLAN®Ochsner Forceps 4161-08
EUDAMED
Class IActive
SCANLAN® Endoscopic Micro Scissors 9009-718SCN
EUDAMED
Class IActive
SCANLAN® Cushing Forceps 4004-56AS
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-928N
EUDAMED
Class IActive
SCANLAN® Sylet for Sundt Suction Tip 9009-928-3N
EUDAMED
Class IActive
SCANLAN® McIndoe Tissue Forceps 4004-63N
EUDAMED
Class IActive
SCANLAN® SUNDT™ Graduated Suction System 9009-980N
EUDAMED
Class IActive
SCANLAN® Puskas™ Premier™ Micro Scissors 7007-514N
EUDAMED
Class IActive
SCANLAN® Endoscopic Fine Needle Holder 9009-380N-12C
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-932N
EUDAMED
Class IActive
SCANLAN® Grasping Forceps 4906-27
EUDAMED
Class IActive
SCANLAN® Puskas Titanium Micro Forceps Q27036-34
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-788N
EUDAMED
Class IActive
SCANLAN® Kerrison Ronguer Q2364-8
EUDAMED
Class IActive
SCANLAN® Bayonet Titanium Micro Forceps Q2562-3
EUDAMED
Class IActive
SCANLAN® Vannas Micro Scissors Q2130-7
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-14N
EUDAMED
Class IActive
SCANLAN® Titanium Resano Forceps 3240-17T
EUDAMED
Class IActive
SCANLAN® Rochester‑Pean Forceps 4141-09
EUDAMED
Class IActive
SCANLAN® Diethrich‑Potts Scissors 7007-254SCN
EUDAMED
Class IActive
SCANLAN®MEMORY Mirror Instrument 8008-420-4
EUDAMED
Class IActive
SCANLAN® CardioVasive™ Knot Tier/Pusher 9009-827
EUDAMED
Class IActive
SCANLAN® Tumor Grasping Forceps 3049-92N
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-212N
EUDAMED
Class IActive
SCANLAN® Bayonet Titanium Micro Forceps Q2563-3
EUDAMED
Class IActive
SCANLAN® Heifetz Micro Forceps 2802-02
EUDAMED
Class IActive
SCANLAN® Mounding Resano Clamp 2222-10
EUDAMED
Class IActive
SCANLAN® Minimally Invasive Micro Scissors 9009-716SCN
EUDAMED
Class IActive
SCANLAN® Gerald DeBakey Forceps 3003-740N
EUDAMED
Class IActive
SCANLAN® Micro Forceps 4004-261N
EUDAMED
Class IActive
SCANLAN® Thoracoscopic Chitwood DeBakey Clamp Q28056-9
EUDAMED
Class IActive
SCANLAN® Variable Suction Rotatable Tips 9009-981N
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-914N
EUDAMED
Class IActive
SCANLAN® Thumb Dressing Forceps 3010-04
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-224N
EUDAMED
Class IActive
SCANLAN® Custom Occlusion Clamp Q28100-2
EUDAMED
Class IActive

Related Companies

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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