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US
Last updated May 23, 2026
What Hdc Corp. makes
Hdc Corp. manufactures orthodontic anchoring screws, reusable dental and maxillofacial surgical procedure kits that are non‑medicated, and reusable surgical screwdrivers, with the SPIDER SCREW being a representative device.
These products fall under Class I and Class II device classifications and are listed in the FDA 510(k) and FDA UDI registries; 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 type of devices does Hdc Corp manufacture?
Hdc Corp manufactures orthodontic anchoring screws, dental/maxillofacial surgical procedure kits, and surgical screwdrivers, as seen with their SPIDER SCREW device, which falls under these categories.
Where is Hdc Corp based?
Hdc Corp is based in the US, as indicated by their country of origin.
Which registries list Hdc Corp's devices?
Hdc Corp's devices are listed in the fda_510k and fda_udi registries, which track medical devices.
How are Hdc Corp's devices classified?
Hdc Corp's devices are classified as either Class I or Class II devices, which determines their level of regulatory control.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- 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
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Catalogue (62)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Neuro-Trace Iii Kit, Neuro-Trace Iii Regional Block Cable, Neuro-Trace Iii Nerve Mapping Probe, Neuro-Trace Iii Nerve Bg | K023342 | FDA 510(k) | Class II | Active |
| J-Cath(tm) | K875171 | FDA 510(k) | Class II | Active |
| V-Cath Picc (peripherally Inserted Central Catheter) | K983916 | FDA 510(k) | Class II | Active |
| Hdc Chemo-Port (vascular) | K853332 | FDA 510(k) | Class II | Active |
| Safe-T-Peel Safety Needle/Introducer, Models 350-300 S, 360-300's, 380-300's, 390-300's | K022099 | FDA 510(k) | Class II | Active |
| Epicath | K862358 | FDA 510(k) | Class II | Active |
| Hdc Silcath Subclavian Catheter Percutaneous Inser | K851078 | FDA 510(k) | Class II | Active |
| Hdc Vadd (vascular Access Device) Tunneler | K951098 | FDA 510(k) | Class II | Active |
| Modification To V-Cath Poly Picc | K033853 | FDA 510(k) | Class II | Active |
| Chemo-Port Non-Coring Needles | K873165 | FDA 510(k) | Class II | Active |
| Neurotrac | K831715 | FDA 510(k) | Class II | Active |
| V-Cath Picc (peripherally Inserted Central Catheter) See Appendix 1 | K983409 | FDA 510(k) | Class II | Active |
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