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Integra Microfrance

US

Last updated May 26, 2026

What Integra Microfrance makes

Integra Microfrance manufactures reusable surgical instruments, including rigid endoscopic tissue manipulation forceps, non-illuminating suction cannulas, laparoscopic trocar blades, general-purpose surgical scissors, ENT elevators, monopolar electrosurgical handpieces, soft-tissue manipulation forceps, and hand-held retractors. These tools are designed for use in endoscopic, laparoscopic, and general surgical procedures.

The company’s products are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Integra Microfrance manufacture?

Integra Microfrance specializes in reusable surgical instruments used across various procedures. Their product line includes rigid endoscopic tissue manipulation forceps, non-illuminating suction cannulas for surgical/emergency use, laparoscopic trocar blades, general-purpose surgical scissors, ENT elevators, monopolar electrosurgical handpieces, soft-tissue manipulation forceps (scissors-like), and hand-held retractors. These tools are designed for endoscopic, laparoscopic, and general surgery applications.

Where is Integra Microfrance based?

Integra Microfrance is headquartered in the United States. The company’s location is relevant for regulatory inquiries, as it may influence jurisdiction-specific requirements for device authorization.

Which regulatory registries list Integra Microfrance’s devices?

Integra Microfrance’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for commercial distribution in the U.S., ensuring traceability and compliance with regulatory standards.

How are Integra Microfrance’s devices classified under FDA regulations?

Integra Microfrance’s devices fall under FDA’s Class I and Class II categories. Class I generally includes low-risk devices requiring general controls, while Class II involves special controls to ensure safety and effectiveness. The classification determines the regulatory pathway for authorization, with Class II often requiring pre-market notifications or other submissions.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
+1(800)654-2873
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
276593071

Catalogue (2622)

Page 32 of 53
DeviceModel / ReferenceRegistriesClassStatus
MicroFrance® CP314-14
FDA UDI
Class IActive
MicroFrance® MCLS59
FDA UDI
Class IActive
MicroFrance® MCL828C
FDA UDI
Class IActive
MicroFrance® MCEN68BDG
FDA UDI
Class IActive
Integra® MicroFrance® CEV566
FDA UDI
Class IIActive
MicroFrance® CEV9646B5U
FDA UDI
Class IIActive
MicroFrance® MCO311-3-5
FDA UDI
Class IActive
Integra® MicroFrance® CEV407I
FDA UDI
Class IIActive
Integra® MicroFrance® CEV155-1
FDA UDI
Class IIActive
MicroFrance® CP826-1
FDA UDI
Class IActive
MicroFrance® 7726MF
FDA UDI
Class IActive
MicroFrance® MCLS47
FDA UDI
Class IActive
Integra® CEV611T1U
FDA UDI
Class IIActive
MicroFrance® CEV392G24
FDA UDI
Class IIActive
MicroFrance® MCOR30
FDA UDI
Class IActive
MicroFrance® CP823-5
FDA UDI
Class IActive
MicroFrance® 3714098
FDA UDI
Class IActive
MicroFrance® MCEN156
FDA UDI
Class IActive
MicroFrance® CM131
FDA UDI
Class IIActive
MicroFrance® MCSK6
FDA UDI
Class IActive
MicroFrance® CP975A
FDA UDI
Class IActive
Integra® MicroFrance® CEV145-6
FDA UDI
Class IIActive
MicroFrance® 7844T5L30
FDA UDI
Class IActive
Integra® MicroFrance® CEV643I
FDA UDI
Class IIActive
Integra® MicroFrance® CEVA112
FDA UDI
Class IIActive
Integra® MicroFrance® CEV622I
FDA UDI
Class IIActive
MicroFrance® CP611
FDA UDI
Class IActive
MicroFrance® MCL291FD
FDA UDI
Class IActive
MicroFrance® MCLP80
FDA UDI
Class IActive
MicroFrance® MCL83-1
FDA UDI
Class IActive
MicroFrance® 1375210
FDA UDI
Class IActive
MicroFrance® M815B
FDA UDI
Class IActive
MicroFrance® MCL-S22
FDA UDI
Class IActive
MicroFrance® 7805-11
FDA UDI
Class IActive
MicroFrance® 3714025
FDA UDI
Class IActive
Integra® MicroFrance® CEV607
FDA UDI
Class IIActive
MicroFrance® 7762-2
FDA UDI
Class IActive
MicroFrance® 7874MF-25
FDA UDI
Class IActive
MicroFrance® MCOS33
FDA UDI
Class IActive
MicroFrance® CP919
FDA UDI
Class IActive
MicroFrance® MCL37DF
FDA UDI
Class IActive
MicroFrance® MCO667
FDA UDI
Class IActive
MicroFrance® CP613
FDA UDI
Class IActive
MicroFrance® MCO981
FDA UDI
Class IActive
MicroFrance® MCM973D3
FDA UDI
Class IActive
MicroFrance® MCEN130
FDA UDI
Class IActive
MicroFrance® MCM7BISR
FDA UDI
Class IActive
MicroFrance® MCL37G
FDA UDI
Class IActive
MicroFrance® CEV720BRUC
FDA UDI
Class IIActive
MicroFrance® MCO221MO
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Integra Microfrance Sas SAINT AUBIN LE MONIAL Auvergne-Rhone-Alpes · FR FEI 3003249645