UNITY
- Primary DI
- 18257200032587
- Brand
- UNITY
- Company
- Orthofix US LLC
- Model
- 43-1091
- Device description
- UNITY LX SYSTEM CASE
- Published
- 2026-07-17
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| FSM | TRAY, SURGICAL, INSTRUMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| FSM | Tray, Surgical, Instrument | General, Plastic Surgery | 1 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K211712 | 000 |
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K211712 | 000 | 3° Anterior Cervical Plating System, Reliant Anterior Cervical Plating System, Unity Lumbosacral Fixation System, Hallmark Anterior Plate System, NewBridge Laminoplasty Fixation System, CETRA Anterior Cervical Plate System | Orthofix US, LLC | 2022-02-11 | KWQ |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 18257200032587 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 18257200032587 | 18257200032587 |
GMDN Terms#
| Term | Definition |
|---|---|
| Instrument tray, reusable | A container intended to provide a suitable platform for placing/containing many medical/surgical/dental instruments and related items for use during a clinical procedure; it might, in addition, be used during, but not dedicated to, reprocessing/sterilization procedures. It is a receptacle in one of a variety of designs, typically with moulded positions for placing the instruments; it might include a lid and/or removable identification tags. This is a reusable device. |
Contacts#
| Phone | |
|---|---|
| +1(800)527-0404 | customerservice@orthofix.com |
Regulatory Flags#
- DUNS number
- 927083808
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 18257200028177 | PHOENIX SFS | 20-0101 | 2026-07-17 | |
| 18257200028207 | PHOENIX SFS | 20-0120 | 2026-07-17 | |
| 18257200028917 | FIREBIRD SFS | 20113073 | 2026-07-17 | |
| 18257200028924 | FIREBIRD SFS | 20113074 | 2026-07-17 | |
| 18257200028931 | FIREBIRD SFS | 20113075 | 2026-07-17 | |
| 18257200028948 | FIREBIRD SFS | 20113076 | 2026-07-17 | |
| 18257200028955 | FIREBIRD SFS | 20113078 | 2026-07-17 | |
| 18257200028979 | FIREBIRD SFS | 20113080 | 2026-07-17 | |
| 18257200028986 | FIREBIRD SFS | 20113081 | 2026-07-17 | |
| 18257200028993 | FIREBIRD SFS | 20113082 | 2026-07-17 | |
| 18257200029006 | FIREBIRD SFS | 20113083 | 2026-07-17 | |
| 18257200029013 | FIREBIRD SFS | 20113084 | 2026-07-17 | |
| 18257200029020 | FIREBIRD SFS | 20113085 | 2026-07-17 | |
| 18257200029280 | FIREBIRD SFS | 20114797 | 2026-07-17 | |
| 18257200029846 | FIREBIRD SFS | 30110025 | 2026-07-17 | |
| 18257200029853 | FIREBIRD SFS | 30110026 | 2026-07-17 | |
| 18257200029860 | FIREBIRD SFS | 30110027 | 2026-07-17 | |
| 18257200029877 | FIREBIRD SFS | 30110028 | 2026-07-17 | |
| 18257200029884 | FIREBIRD SFS | 30110029 | 2026-07-17 | |
| 18257200029945 | FIREBIRD SFS | 30110035 | 2026-07-17 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 07640221370884 | TRYPTIK® Ti | SpineArt SA | FSM | 2026-08-27 |
| 07613327630602 | Mako | MAKO SURGICAL CORP. | FSM | 2026-08-25 |
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