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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 47 of 58
DeviceModel / ReferenceRegistriesClassStatus
SCANLAN® Dilators 9009-49E
EUDAMEDFDA UDI
Class IIActive
SCANLAN® Jacobson Micro Scissors 7007-456
FDA UDI
Class IActive
SCANLAN® Forceps Q2358-3
EUDAMEDFDA UDI
Class IActive
SCANLAN® Suction System Devices 9009-929
EUDAMEDFDA UDI
Class IIActive
Scanlan® VASCU-STATT® Plus aprox s-use bulldog clamp w/Gentle-Jaw™ surface 1001-561
FDA UDI
Class IActive
SCANLAN® Forceps 4004-11
FDA UDI
Class IActive
Scanlan® VASCU-STATT® Applier 1001-506M
EUDAMEDFDA UDI
Class IActive
SCANLAN® Stainless Steel Scissors Q31065-7
EUDAMEDFDA UDI
Class IActive
Scanlan® 9009-420-12
EUDAMEDFDA UDI
Class IIActive
Jacobson Micro Needle Holder Flat Handle 6006-114
FDA UDI
Class IActive
Scanlan® 3003-76
EUDAMEDFDA UDI
Class IIActive
Scanlan® 3003-612
EUDAMEDFDA UDI
Class IIActive
Scanlan® 3786-27
FDA UDI
Class IIActive
SCANLAN® Scanturian™ MIS Instrument 9019-450-17
FDA UDI
Class IIActive
Scanlan® 7007-31
EUDAMEDFDA UDI
Class IActive
SCANLAN® Scissors 7007-266
EUDAMEDFDA UDI
Class IActive
SCANLAN® Minimally Invasive Instrumentation 9009-226-04
EUDAMEDFDA UDI
Class IActive
SCANLAN® Jacobson Micro Scissors 7007-154
EUDAMEDFDA UDI
Class IActive
SCANLAN® Clamp Q29011-2
EUDAMEDFDA UDI
Class IIActive
SCANLAN® Instrumentation 9009-823-16
FDA UDI
Class IActive
Scanlan® 3003-68
EUDAMEDFDA UDI
Class IIActive
Scanlan® 2002-38
EUDAMEDFDA UDI
Class IIActive
SCANLAN® Super Cut™ 7007-216SC
EUDAMEDFDA UDI
Class IActive
SCANLAN® Advantage™ Badie™ Suction Bipolar Forceps 3787-25
FDA UDI
Class IIActive
SCANLAN® Super Cut™ 7007-403
FDA UDI
Class IActive
SCANLAN® Needle Holders 3003-394
EUDAMEDFDA UDI
Class IActive
SCANLAN® Forceps 4004-206
EUDAMEDFDA UDI
Class IActive
SCANLAN® Titanium Forceps 3003-806
EUDAMEDFDA UDI
Class IActive
Scanlan® 3003-640
FDA UDI
Class IIActive
SCANLAN® Titanium Clamp 3003-619
EUDAMEDFDA UDI
Class IActive
SCANLAN® Dilators 9009-94
EUDAMEDFDA UDI
Class IIActive
SCANLAN® Jacobson Micro Scissors 7007-152
FDA UDI
Class IActive
SCANLAN® Ultra Sharp® 7007-284
EUDAMEDFDA UDI
Class IActive
SCANLAN® Super Cut™ and Ultra Sharp® Scissors 7007-215-2
EUDAMEDFDA UDI
Class IActive
SCANLAN® Super Cut™ 7007-205
EUDAMEDFDA UDI
Class IActive
SCANLAN® Needle Holders 3003-397
EUDAMEDFDA UDI
Class IActive
SCANLAN® Super Cut™ 7007-244SC
FDA UDI
Class IActive
Scanlan® SURG-I-PAW® Instrument Covers 1001-74B
FDA UDI
Class IActive
SCANLAN® Forceps / Haemostats / Clamps 4635-06
EUDAMEDFDA UDI
Class IIActive
SCANLAN® Minimally Invasive Instrument COA013-09
FDA UDI
Class IIActive
SCANLAN® Forceps 3010-10
EUDAMEDFDA UDI
Class IActive
SCANLAN® Jacobson Micro Scissors 7007-494-8
FDA UDI
Class IActive
Scanlan® 9009-224-1
EUDAMEDFDA UDI
Class IIActive
Scanlan® 7007-44
EUDAMEDFDA UDI
Class IActive
SCANLAN® Jacobson Micro Scissors 7007-490S
FDA UDI
Class IActive
SCANLAN® Forceps 4004-74
EUDAMEDFDA UDI
Class IActive
Scanlan® VASCU-STATT® II single-use bulldog clamp w/firmer clamping press 1001-529
FDA UDI
Class IActive
SCANLAN® John Ross Tunneler System 9009-34
FDA UDI
Class IActive
SCANLAN® Scanturian™ MIS Instrument 9019-614-17
EUDAMEDFDA UDI
Class IIActive
Scanlan® 9009-310
EUDAMEDFDA UDI
Class IIActive

Related Companies

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Importers

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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