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Sign in to claim this brandHPF SRL
US
Last updated May 23, 2026
What HPF SRL makes
HPF SRL manufactures orthopaedic surgical instruments and tools for hip replacement procedures, including acetabular reamers, osteotome blades, chisel blades, and reusable acetabulum prosthesis trials. Their portfolio also covers power tool attachments like burring and drilling tools, as well as specialized handles and mandrels designed for precision bone resection and acetabular preparation.
All listed devices fall under Class I regulatory classification and are registered in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable U.S. medical device regulations.
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 HPF SRL manufacture?
HPF SRL specializes in orthopaedic surgical instruments and tools primarily used in hip replacement procedures. Their product range includes acetabular orthopaedic reamers for bone preparation, reusable osteotome and chisel blades for cutting bone, acetabulum prosthesis trials for fitting, and power tool attachments like burring and drilling tools. These devices are designed to assist surgeons in precise bone resection and acetabular preparation during hip surgeries.
Where is HPF SRL based, and what does that mean for their devices?
HPF SRL is based in the United States, which means their devices are subject to U.S. medical device regulations. Since they operate domestically, their products must comply with FDA requirements, including registration in the FDA’s Unique Device Identifier (UDI) database. This ensures traceability and adherence to regulatory standards for medical devices in the U.S. market.
Which regulatory registries list HPF SRL’s devices, and why is this important?
HPF SRL’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is critical because it provides a standardized way to identify medical devices throughout their distribution and use. The UDI system helps track devices for safety monitoring, recalls, and compliance verification, ensuring transparency and accountability in the medical device supply chain.
How are HPF SRL’s devices classified under U.S. regulations?
All of HPF SRL’s listed devices fall under Class I regulatory classification in the U.S. This classification is typically assigned to low-risk devices that pose minimal potential harm to patients. Class I devices often require general controls (like proper labeling and manufacturing practices) but may not need pre-market approval, depending on their specific design and risk profile. The classification ensures these tools meet basic safety and effectiveness standards without additional pre-market scrutiny.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 895802853
Catalogue (1199)
Page 20 of 24| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ACETABULAR REAMER EVO 2 D51 mm | H0036555199 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER D43 mm HC | 01.30.10.3243 | FDA UDI | Class I | Active |
| ACETABULAR REAMER D66 mm HC | 01.30.10.3266 | FDA UDI | Class I | Active |
| ACETABULAR REAMER D45 mm HC | 01.30.10.3245 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER D41 mm HC | 9057.20.941 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER D41 mm HC | 01.30.10.3241 | EUDAMEDFDA UDI | Class I | Active |
| Straight Handle Hpf Conn. Zimmer | H0030100050 | EUDAMEDFDA UDI | Class I | Active |
| Blades Support Handle | H0050300099 | EUDAMEDFDA UDI | Class I | Active |
| Drop Ratchet Handle White | H1500030609 | FDA UDI | Class I | Active |
| LIGHTENED TRIAL HEAD D46 mm | H0050051508 | FDA UDI | Class I | Active |
| Depth Gauge | 01.32.10.0292 | EUDAMEDFDA UDI | Class I | Active |
| LIGHTENED TRIAL HEAD D42 mm | H0050051506 | FDA UDI | Class I | Active |
| SHORT ACETABULAR BLADE D50 mm LONG | H0050451169 | EUDAMEDFDA UDI | Class I | Active |
| CARDAN SCREWDRIVER HEX. 3, 5 mm CONN. ZIMMER | H0150005599 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER HM D54 mm HC | 01.30.10.3554 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR BLADE D66 mm SHORT | H0050450319 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER D51 mm HC | 01.30.10.3251 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER HM D76 mm HC | 01.30.10.3576 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER D72 mm HC | 01.30.10.3272 | EUDAMEDFDA UDI | Class I | Active |
| TRIAL CUP D53 mm | 9055.28.453 | EUDAMEDFDA UDI | Class I | Active |
| THIN OSTEOTOME BLADE 127x8 WITH SLOT | H0050300549 | EUDAMEDFDA UDI | Class I | Active |
| Depth Gauge R40 | H0010350199 | EUDAMEDFDA UDI | Class I | Active |
| Drop Ratchet Handle Cannulated White | H1500030659 | FDA UDI | Class I | Active |
| CUP IMPACTOR M8x1 | 01.15.10.0636 | EUDAMEDFDA UDI | Class I | Active |
| Straight Ratched Handle Night Blue | H1500050309 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER HM D48 mm HC | 01.30.10.3548 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER D58 mm HPF | H0030054509 | FDA UDI | Class I | Active |
| TRIAL CUP D42 mm | H0030151009 | FDA UDI | Class I | Active |
| RADIAL OSTEOTOME MEDIAL BLADE 127x12 WITH HOLE | 90300065900 | EUDAMEDFDA UDI | Class I | Active |
| Straight Handle Universal Conn. A.o. Implantcast | H0030770099 | EUDAMEDFDA UDI | Class I | Active |
| TRIAL CUP D62 mm | 9055.28.462 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER EVO 2 D43 mm | H0036554399 | EUDAMEDFDA UDI | Class I | Active |
| Straight Handle M8 Night Blue | H1500050059 | FDA UDI | Class I | Active |
| Drop Ratchet Handle Black | H1500010609 | FDA UDI | Class I | Active |
| Straight Ratched Handle Violet | H1500020309 | FDA UDI | Class I | Active |
| ACETABULAR REAMER EVO D46 mm | H0035554699 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER EVO D66 mm | H0035556699 | EUDAMEDFDA UDI | Class I | Active |
| ACCESSORY CONN. M8x1 | H0034000319 | FDA UDI | Class I | Active |
| TRIAL CUP D39 mm | 9055.28.439 | EUDAMEDFDA UDI | Class I | Active |
| PLANAR CUTTER D57 mm | H0250005799 | FDA UDI | Class I | Active |
| Standard Handle M8 Black | H5000060009 | FDA UDI | Class I | Active |
| ACETABULAR REAMER HM D54 mm HC | H0033005499 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER EVO 2 D52 mm | H0036555299 | EUDAMEDFDA UDI | Class I | Active |
| "T" HANDLE 195 mm CONN. A.O. | 01.11.10.0056 | FDA UDI | Class I | Active |
| THIN OSTEOTOME BLADE 76x20 WITH HOLE | 90300065830 | EUDAMEDFDA UDI | Class I | Active |
| TRIAL CUP D42 mm | 9055.28.442 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER HM D50 mm HC | H0033005099 | EUDAMEDFDA UDI | Class I | Active |
| DRILL BIT D4, 5 mm L=70 mm | 01.10.10.0064 | EUDAMEDFDA UDI | Class I | Active |
| ACETABULAR REAMER D52 mm FC | 01.30.10.3452 | EUDAMEDFDA UDI | Class I | Active |
| RADIAL OSTEOTOME BLADE 127x16 WITH SLOT | H0050300609 | FDA UDI | Class I | Active |
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