Identity
- Trade Name
- OIC Intramedullary Nail System FDA UDI
- Generic Name
- Orthopaedic implant aiming arm FDA UDI
- Device Name
- CARBON HIP DROP FDA UDI
- Model / Reference
- 01-IM22 FDA UDI
- Description
- CARBON HIP DROP FDA UDI
Identifiers
- Primary DI / UDI-DI
- M69601IM220 FDA UDI
- 510(k) Number
- K150655 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Orthopaedic implant aiming arm FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3020 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic implant aiming arm
OIC Intramedullary Nail System by Orthopaedic Implant Company, The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic implant aiming arm.
- ANTEGRADE TARGETING MODULE FEMORAL NAIL SYSTEM — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I
- TARGETING ARM — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I
- Dyna Locking Trochanteric Nail — CG MedTech Co., Ltd. · Class I
- ANTEGRADE FEMORAL NAIL DRIVER — Biomet Orthopedics, Inc. · Class I
- Jig — I.T.S. GmbH · Class I
- ACUFEX — Smith & Nephew, Inc. · Class I
- ENDO - KNEE — Smith & Nephew, Inc. · Class I
- Proximal Humeral Fracture Plate System — Smith & Nephew, Inc. · Class I
Cleared under the same submission
K150655 also covers:
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
- OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE
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 II | Pending data |
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Manufacturer
- Manufacturer
- Orthopaedic Implant Company, The
Sources (1)
- FDA UDI 48ba5a84-89ab-47d1-b08f-abc5a708f88b 35 fields · synced May 30, 2026