Identity
- Trade Name
- Trigon FDA UDI
- Generic Name
- Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
- Device Name
- Instrument: 8mm Trial 6° Transverse PEEK Small Multi Joint Lesser Metatarsal The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as: • Cotton (opening wedge) Osteotomies of the Medial Cuneiform • Evans Lengthening Osteotomies • Subtalar Fusion • First Metatarsal-Cuneiform Lengthening Arthrodesis • Calcaneocuboid Arthrodesis • Calcaneal Z Lengthening Osteotomies • MTP Lengthening Arthrodesis • Lesser Metatarsal-Cuneiform Lengthening Arthrodesis • Navicular-Cuneiform Arthrodesis • Talonavicular Arthrodesis The Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine. FDA UDI
- Model / Reference
- LM-1428T-0806 FDA UDI
- Description
- Instrument: 8mm Trial 6° Transverse PEEK Small Multi Joint Lesser Metatarsal The Trigon HA Stand-Alone Wedge Fixation System is intended to be used for internal bone fixation for bone fractures or osteotomies in the ankle and foot, such as: • Cotton (opening wedge) Osteotomies of the Medial Cuneiform • Evans Lengthening Osteotomies • Subtalar Fusion • First Metatarsal-Cuneiform Lengthening Arthrodesis • Calcaneocuboid Arthrodesis • Calcaneal Z Lengthening Osteotomies • MTP Lengthening Arthrodesis • Lesser Metatarsal-Cuneiform Lengthening Arthrodesis • Navicular-Cuneiform Arthrodesis • Talonavicular Arthrodesis The Trigon HA wedges are intended for use with ancillary fixation. The Trigon HA Stand-Alone Wedge Fixation System is not intended for use in the spine. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810135962780 FDA UDI
- 510(k) Number
- K243231 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic inorganic implant inserter/extractor, reusable
Trigon by Nvision Biomedical Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K243231 also covers:
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
- Trigon — NVISION BIOMEDICAL TECHNOLOGIES, INC
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Nvision Biomedical Technologies, Inc
Sources (1)
- FDA UDI 032d05fd-2b0d-4bd3-aad9-b5e514b5e831 35 fields · synced May 30, 2026