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Sign in to claim this brandJohnson & Johnson International Inc.
US
Last updated September 17, 2026
Part of Johnson & Johnson International
What Johnson & Johnson International Inc. makes
The company manufactures composite-polymer surgical meshes for extra-gynaecological and pelvic organ prolapse procedures, including products like ULTRAPRO and ULTRAPRO ADVANCED. It also produces bioabsorbable polyester sutures, such as PROCEED, and suture retention devices, including the ULTRAPRO COMFORT PLUG. Additional offerings include the ETHICON PHYSIOMESH mesh for pelvic organ prolapse repair.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 Johnson & Johnson International Inc. manufacture?
Johnson & Johnson International Inc. specializes in composite-polymer surgical meshes used for extra-gynaecological and pelvic organ prolapse procedures. Their portfolio includes products like ULTRAPRO and ULTRAPRO ADVANCED for mesh applications, as well as bioabsorbable polyester sutures such as PROCEED. Additionally, they produce suture retention devices like the ULTRAPRO COMFORT PLUG and the ETHICON PHYSIOMESH mesh for pelvic organ prolapse repair. These devices are designed to support tissue repair and structural reinforcement in surgical contexts.
Where is Johnson & Johnson International Inc. based?
Johnson & Johnson International Inc. is headquartered in the United States. This location serves as the primary base for their operations, including research, development, and manufacturing of their medical devices.
Which regulatory registries list devices manufactured by Johnson & Johnson International Inc.?
Devices manufactured by Johnson & Johnson International Inc. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices authorized for use in the United States, allowing healthcare providers and regulators to access critical information about the devices.
How are the devices produced by Johnson & Johnson International Inc. classified under FDA regulations?
The devices produced by Johnson & Johnson International Inc., such as their surgical meshes and sutures, are classified as Class II under FDA regulations. This classification indicates that they pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. Class II devices undergo a premarket notification (510(k)) process to demonstrate substantial equivalence to a legally marketed predicate device.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- xxx.xxx
- —
- —
- [email protected]
- Phone
- +1(877)384-4266
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 372587696
Catalogue (86)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ultrapro | UMM3 | FDA UDI | Class II | Active |
| Proceed | PCDW1 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | OPHY1010 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | OPHY1525 | FDA UDI | Class II | Active |
| Ultrapro | UPPM2 | FDA UDI | Class II | Active |
| Artisyn | ARTY | FDA UDI | Class II | Active |
| Proceed | PCDL1 | FDA UDI | Class II | Active |
| Ethicon | PCP30 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | PHY1515Q | FDA UDI | Class II | Unknown |
| Proceed | PCDR1 | FDA UDI | Class II | Active |
| Ethicon | PCP50 | FDA UDI | Class II | Active |
| Proceed | PCDN1 | FDA UDI | Class II | Active |
| Vicryl | VM106K | FDA UDI | Class II | Unknown |
| Ultrapro Advanced | UPA31015 | FDA UDI | Class II | Active |
| Ultrapro Advanced | UPA1530 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | OPHY1010 | FDA UDI | Class II | Active |
| Proceed | PCDG1 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | OPHY1520 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | PHY2025V | FDA UDI | Class II | Unknown |
| Ultrapro Advanced | UPA3612 | FDA UDI | Class II | Active |
| Ultrapro | UPPM6 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | OPHY1215 | FDA UDI | Class II | Active |
| Ultrapro Comfort Plug | UPLUG551 | FDA UDI | Class II | Active |
| Ultrapro | UHSL6 | FDA UDI | Class II | Active |
| Ultrapro Comfort Plug | UPLUG403 | FDA UDI | Class II | Unknown |
| Ultrapro Advanced | UPA37615 | FDA UDI | Class II | Active |
| Ultrapro | UHSOV | FDA UDI | Class II | Active |
| Ultrapro Comfort Plug | UPLUG406 | FDA UDI | Class II | Active |
| Ultrapro Comfort Plug | UPLUG403 | FDA UDI | Class II | Active |
| Vicryl | VM102K | FDA UDI | Class II | Unknown |
| Ethicon Physiomesh | OPHY1215 | FDA UDI | Class II | Active |
| Ethicon Physiomesh | OPHY2536 | FDA UDI | Class II | Active |
| Vicryl Rapide | VR2218 | FDA UDI | Class II | Active |
| Proceed | PVPS | FDA UDI | Class II | Active |
| Ultrapro | UHSL | FDA UDI | Class II | Active |
| Proceed | PCDD1 | FDA UDI | Class II | Active |
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