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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 4 of 58
DeviceModel / ReferenceRegistriesClassStatus
SCANLAN® Vascular Forceps Q2422-5
EUDAMED
Class IActive
SCANLAN®Ochsner Forceps 4160-07
EUDAMED
Class IActive
SCANLAN® Premier™ flat spring style handle 7007-542N
EUDAMED
Class IActive
SCANLAN® Russian Forceps 3431-06
EUDAMED
Class IActive
SCANLAN® Metzenbaum Scissors 7007-216-2SCN
EUDAMED
Class IActive
SCANLAN® Rochester‑Pean Forceps 4140-09
EUDAMED
Class IActive
SCANLAN® DeBakey Needle Pulling Tissue Forceps 4004-37N
EUDAMED
Class IActive
SCANLAN® Thumb Dressing Forceps 3000-06
EUDAMED
Class IActive
SCANLAN® Lower Kidney Transplant Clamp Q2578-2
EUDAMED
Class IActive
SCANLAN® Premier™ flat spring style handle 7007-544N
EUDAMED
Class IActive
SCANLAN® Cardiovasive™ Metzenbaum Super Cut™ Scissors Q2111-9
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-320N
EUDAMED
Class IActive
SCANLAN® Metzenbaum Scissors 7007-216SCN
EUDAMED
Class IActive
SCANLAN® Meniscus Punch Forceps 4927-45
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-926N
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-96N
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-96T
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forcep 3003-720N
EUDAMED
Class IActive
SCANLAN® Lillehei‑Potts Scissors 7007-268SCN
EUDAMED
Class IActive
SCANLAN® Allis Tissue Forceps 4813-04
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps Q26008-34N
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 4004-245T
EUDAMED
Class IActive
SCANLAN® Tumor Grasping Forceps 3049-90N
EUDAMED
Class IActive
SCANLAN® Jacobson Retrograde Knife/Dissector 3784-451N
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 3003-712N
EUDAMED
Class IActive
SCANLAN® Gerald Forceps 4004-244N
EUDAMED
Class IActive
SCANLAN® Jacobson Micro Scissors Flat Handle 7007-546-8
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-04N
EUDAMED
Class IActive
SCANLAN® Foerster Clamp Q34030-9-1
EUDAMED
Class IActive
SCANLAN® Rochester‑Pean Forceps 4141-06
EUDAMED
Class IActive
SCANLAN® Sylet for Sundt Suction Tip 9009-929-3N
EUDAMED
Class IActive
SCANLAN® Yasargil‑Type Temporary Clip Q25022-8
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps 4004-95T
EUDAMED
Class IActive
SCANLAN® Bonn Model Peripheral Forceps Q2337-4
EUDAMED
Class IActive
SCANLAN® Thumb Dressing Forceps 3000-05
EUDAMED
Class IActive
SCANLAN® Foerster Forcep 4559-09
EUDAMED
Class IActive
SCANLAN® Variable Suction Rotatable Tips 9009-967N
EUDAMED
Class IActive
SCANLAN® CardioVasive™ /Thoracoscopic Babcock Clamp 9909-920B
EUDAMED
Class IActive
SCANLAN® Variable Suction Rotatable Tips 9009-961N
EUDAMED
Class IActive
SCANLAN® Finesse Micro Forceps 2924-00
EUDAMED
Class IActive
SCANLAN® Variable Suction Rotatable Tips 9009-941N
EUDAMED
Class IActive
SCANLAN® Titanium Micro Forceps 3003-934N
EUDAMED
Class IActive
SCANLAN® Ryder Needle Holder 3003-432N
EUDAMED
Class IActive
SCANLAN® Titanium Micro forceps Q2556-3
EUDAMED
Class IActive
SCANLAN® Tissue Forceps 3120-06
EUDAMED
Class IActive
SCANLAN® Heifetz™ Temporary Occlusion Clip 3795-28-XM
EUDAMED
Class IActive
SCANLAN® MEMORY Calipers 8008-400E
EUDAMED
Class IActive
SCANLAN® Suction Cleaning Stylet 4004-126N
EUDAMED
Class IActive
SCANLAN® Dennis Micro Forceps Q2349-4
EUDAMED
Class IActive
SCANLAN® Stern Chest Passer 4004-186-1
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