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SOFRADIM PRODUCTION

US

Last updated May 24, 2026

What SOFRADIM PRODUCTION makes

The company manufactures extra-gynaecological surgical meshes, including composite-polymer, synthetic polymer (both non-bioabsorbable and bioabsorbable), and collagen-based bioabsorbable variants. These products are designed for surgical applications requiring tissue reinforcement or repair, such as hernia repair or pelvic organ prolapse correction. Device examples include Parietex, ProGrip, Symbotex, Versatex, Parietene DS, and Parietene.

The portfolio consists of devices classified as Class II and Class III under regulatory frameworks, with submissions documented via FDA 510(k) and FDA Unique Device Identification (UDI) listings. These products are authorised for use in the United States, where the manufacturer is based.

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 Sofradim Production manufacture?

Sofradim Production specialises in extra-gynaecological surgical meshes, which are used primarily for tissue reinforcement or repair in procedures like hernia repair or pelvic organ prolapse correction. Their portfolio includes meshes made from composite polymers, synthetic polymers (both non-bioabsorbable and bioabsorbable), and collagen-based bioabsorbable materials without antimicrobial properties.

Where is Sofradim Production based, and where are their devices authorised for use?

Sofradim Production is headquartered in the United States. Their devices are authorised for use in the US, where regulatory submissions—such as FDA 510(k) clearances and FDA Unique Device Identification (UDI) listings—are documented. This reflects the company’s focus on compliance with US regulatory requirements.

Which regulatory registries or databases list Sofradim Production’s devices?

Sofradim Production’s devices are documented in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identification (UDI) system. These registries track submissions and classifications required for device authorisation in the US, ensuring transparency in their regulatory status.

How are Sofradim Production’s devices classified under regulatory frameworks?

Sofradim Production’s devices fall into two regulatory classes: Class II and Class III. Class II devices typically pose moderate risk and require special controls beyond general controls, while Class III devices are higher-risk and generally require premarket approval due to insufficient data to assure safety and effectiveness through other means. The classification depends on factors like the device’s intended use and potential risks.

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

Information

Country
US
Address
—
Website
covidien.com
LinkedIn
—
Facebook
—
Phone
+1(508)261-8000
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
576342646

Catalogue (296)

Page 2 of 6
DeviceModel / ReferenceRegistriesClassStatus
Parietex PCO1510FX
FDA UDI
Class IIActive
Permacol P100104
FDA UDI
Class IIActive
Dextile DXT1309AL
FDA UDI
Class IIActive
Parietex PCO12FX
FDA UDI
Class IIActive
Parietex TCM3015
FDA UDI
Class IIUnknown
Parietene DS PPDS3530
FDA UDI
Class IIActive
ProGrip LPG1612AL
FDA UDI
Class IIActive
Permacol P050205
FDA UDI
Class IIActive
Parietex TCM1106X3
FDA UDI
Class IIUnknown
Versatex VTX1515MX3
FDA UDI
Class IIActive
Parietene PPM4530
FDA UDI
Class IIActive
Parietene DS PPDS12X3
FDA UDI
Class IIActive
Parietex TCM4530
FDA UDI
Class IIUnknown
Parietene PPMK1106X3
FDA UDI
Class IIActive
Parietex TECT1510AL
FDA UDI
Class IIActive
Parietex PCO3728FX
FDA UDI
Class IIActive
Duatene DTN07R
FDA UDI
Class IIUnknown
Permacol P050308
FDA UDI
Class IIUnknown
Permacol P100510
FDA UDI
Class IIActive
Parietex PCOPM15H50
FDA UDI
Class IIActive
Permacol P151015
FDA UDI
Class IIActive
Parietex PCO2H4
FDA UDI
Class IIActive
Permacol CRCRP510
FDA UDI
Class IIUnknown
Dextile DXT1612AL
FDA UDI
Class IIActive
Enduragen 89223
FDA UDI
Class IIActive
Parietex TECT1612AL
FDA UDI
Class IIActive
Parietex PCO6VP
FDA UDI
Class IIActive
Dextile DXT1510AL
FDA UDI
Class IIActive
Parietene PPM1508X6
FDA UDI
Class IIActive
Parietex TEC1515
FDA UDI
Class IIActive
ProGrip LPG1612
FDA UDI
Class IIActive
Duatene DTN10RX3
FDA UDI
Class IIUnknown
Parietex PCOPM20
FDA UDI
Class IIUnknown
Parietene DS PPDS2015
FDA UDI
Class IIActive
Parietex PCO8VP
FDA UDI
Class IIUnknown
Parietene PPM2020X3
FDA UDI
Class IIActive
Parietex TEC1410DP
FDA UDI
Class IIUnknown
Permacol CRCRP505
FDA UDI
Class IIUnknown
Parietex TCM1510
FDA UDI
Class IIUnknown
Transorb TSB2020
FDA UDI
Class IIActive
Symbotex SYM3420E
FDA UDI
Class IIActive
Symbotex SYM15
FDA UDI
Class IIActive
Symbotex SYM3728F
FDA UDI
Class IIActive
Parietex TECR1515
FDA UDI
Class IIActive
ProGrip TEM1409GR
FDA UDI
Class IIActive
Symbotex SYM2015F
FDA UDI
Class IIActive
Enduragen 89224
FDA UDI
Class IIActive
Parietene DS PPDS15X3
FDA UDI
Class IIActive
Parietex PCO3020OSX
FDA UDI
Class IIActive
Parietex TCM1515
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

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

  • Sofradim Production TREVOUX Auvergne-Rhone-Alpes · FR FEI 3003521774