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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 8 of 58
DeviceModel / ReferenceRegistriesClassStatus
SCANLAN® Dennis Micro Forceps 4004-224T
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-902N
EUDAMED
Class IActive
SCANLAN® Dura Forceps 3160-08
EUDAMED
Class IActive
SCANLAN® Micro W.H. Stainless Steel Q-2566-6
EUDAMED
Class IActive
SCANLAN® Titanium DeBakey Forceps Q29025-34
EUDAMED
Class IActive
SCANLAN® Kerrison Ronguer Q2363-8
EUDAMED
Class IActive
SCANLAN® Stern Chest Passer 4004-189D
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-936N
EUDAMED
Class IActive
SCANLAN® Metzenbaum Scissors Q28032-7
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-22N
EUDAMED
Class IActive
SCANLAN® Yasargil‑Type Temporary Clip 3786-22N
EUDAMED
Class IActive
SCANLAN® Ryder Needle Holder 3003-434N
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-786N
EUDAMED
Class IActive
SCANLAN® Duval Intestinal Lung Clamp 4550-07
EUDAMED
Class IActive
SCANLAN® Papillary Muscle Clamp 4373-11
EUDAMED
Class IActive
SCANLAN® Metzenbaum Scissors 7007-216-1SCN
EUDAMED
Class IActive
SCANLAN® Thumb Dressing Forceps 3010-05
EUDAMED
Class IActive
SCANLAN® Finesse Micro Forceps 2931-00
EUDAMED
Class IActive
SCANLAN® Kocher Intestinal Clamp 4506-11
EUDAMED
Class IActive
SCANLAN® Thumb Forceps 4004-80S
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-916N
EUDAMED
Class IActive
SCANLAN® Micro Forceps 4004-261T
EUDAMED
Class IActive
SCANLAN® Thumb Dressing Forceps 3000-07
EUDAMED
Class IActive
SCANLAN® Multi-Purpose DeBakey Clamp Q29009-2
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4404-228
EUDAMED
Class IActive
SCANLAN® Crile Forceps 4111-06
EUDAMED
Class IActive
SCANLAN® Rochester‑Pean Forceps 4140-07
EUDAMED
Class IActive
SCANLAN® Tumor Grasping Forceps 3003-823N
EUDAMED
Class IActive
SCANLAN®Varco Forcep 4361-08
EUDAMED
Class IActive
SCANLAN® Rochester‑Pean Forceps 4141-08
EUDAMED
Class IActive
SCANLAN® DeBakey‑Cooley Forceps 4377-08N
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-08E
EUDAMED
Class IActive
SCANLAN® Grasping Forceps 4917-45
EUDAMED
Class IActive
SCANLAN® Premier™ Jacobson Micro Scissors 7007-510N
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-18E
EUDAMED
Class IActive
SCANLAN® Jacobson Micro Scissors round handle 7007-590-8
EUDAMED
Class IActive
SCANLAN® Titanium Dennis Micro Forceps Q2326-3
EUDAMED
Class IActive
SCANLAN® Allis Tissue Forceps 4813-08
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-24E
EUDAMED
Class IActive
SCANLAN® Finesse Micro Forceps 2922-00
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-18N
EUDAMED
Class IActive
SCANLAN® Micro Kitzmiller Clamp 3003-630N
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 4004-238N
EUDAMED
Class IActive
SCANLAN® Debakey Needle Pulling Tissue Forceps Q25008-4
EUDAMED
Class IActive
SCANLAN® Irrigating Stylet for Suction Forceps 4004-127N
EUDAMED
Class IActive
SCANLAN® Premier™ round spring style handle 7007-596N
EUDAMED
Class IActive
SCANLAN® Premier™ Jacobson Micro Scissors 7007-539N
EUDAMED
Class IActive
SCANLAN® Backhaus Towel Clamp 4453-04
EUDAMED
Class IActive
SCANLAN® Grasping Forceps 4916-45
EUDAMED
Class IActive
SCANLAN® Cushing Forceps 4004-56S
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