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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 58 of 58
DeviceModel / ReferenceRegistriesClassStatus
SCANLAN® SURG-I-BAND® color coding 1001-1072
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-964
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-968
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-914
EUDAMEDFDA UDI
Class IActive
SCANLAN® SURG-I-BAND® color coding 1001-99
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-909
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-971
EUDAMEDFDA UDI
Class IActive
SCANLAN® SURG-I-BAND® color coding 1001-1061
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-931
EUDAMEDFDA UDI
Class IActive
SCANLAN® SURG-I-BAND® color coding 1001-1046
EUDAMEDFDA UDI
Class IActive
SCANLAN® TIP-GUARD™ instrument protectors 1001-403
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-972
EUDAMEDFDA UDI
Class IActive
SCANLAN® V.I.P™ instrument sterilization trays 2135-03
EUDAMEDFDA UDI
Class IActive
SCANLAN® EASY-TAG™ tracking system 1001-969
EUDAMEDFDA UDI
Class IActive
SCANLAN® SURG-I-BAND® color coding 1001-1022
EUDAMEDFDA UDI
Class IActive

Related Companies

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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