Identity
- Trade Name
- Dymaxeon FDA UDI
- Generic Name
- Orthopaedic implant/instrument assembling device FDA UDI
- Device Name
- Round Handle - Quick Connect FDA UDI
- Model / Reference
- 05.5 FDA UDI
- Description
- Round Handle - Quick Connect FDA UDI
Identifiers
- Catalog Number
- 77.2065 FDA UDI
- Primary DI / UDI-DI
- 00815500023547 FDA UDI
- 510(k) Number
- K121786 FDA UDI
- FDA Product Code
- NKB FDA UDIMNI FDA UDIMNH FDA UDI
- GMDN Term
- Orthopaedic implant/instrument assembling device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3070 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Conditional FDA UDI
Category: Orthopaedic implant/instrument assembling device
Dymaxeon by Back 2 Basic Direct, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic implant/instrument assembling device.
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Cleared under the same submission
K121786 also covers:
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
- Dymaxeon — BACK 2 BASIC DIRECT, LLC
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Back 2 Basic Direct, Llc
Sources (1)
- FDA UDI a2110899-2e07-4432-9d81-86ec85f06d2b 36 fields · synced Jun 6, 2026