FDA.reportPublic FDA data

Apex

Primary DI
05391529582531
Brand
Apex
Company
ORTHOXEL DESIGNATED ACTIVITY COMPANY
Model
INS-1040
Catalog number
INS-1040
Device description
Fracture Reduction Tool
Published
2021-01-29
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LXHOrthopedic Manual Surgical Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05391529582531PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05391529582531053915295825315391529582531

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone-reduction toolA hand-held manual surgical instrument that is fed down the intramedullary canal of a long bone (e.g., the femur) to help reposition a fracture where the two sections are out of alignment to achieve reduction for consequent reaming and nailing of the bone. It is typically a short cylindrical device with a protruding pointed tip (straight or angled) and which is secured to the distal end of a long, thin, flexible rod/shaft having a handle at the proximal end. It is pressed down the intramedullary canal to the fracture site and the surgeon manipulates the alignment, reducing the bone fragments under image-intensifier control. It is made of high-grade stainless steel. This is a reusable device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Ambient Storage and Handling

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
646-661-3167customercare@orthoxel.com

Regulatory Flags#

DUNS number
985596830
Device count
1
DM exempt
true
Premarket exempt
true
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
05391529588502ApexE04-020E04-0202022-08-17
05391529582128ApexE02-000E02-0002022-08-10
05391529582135ApexE02-005E02-0052022-08-10
05391529582142ApexE02-010E02-0102022-08-10
05391529582159ApexE02-015E02-0152022-08-10
05391529582166ApexE02-020E02-0202022-08-10
05391529582173ApexLE02-000LE02-0002022-08-10
05391529588465ApexE04-000E04-0002022-02-23
05391529588472ApexE04-005E04-0052022-02-23
05391529588489ApexE04-010E04-0102022-02-23
05391529588496ApexE04-015E04-0152022-02-23
05391529588519ApexLE04-000LE04-0002022-02-23
05391529585099ApexE03-000E03-0002021-02-05
05391529585105ApexE03-005E03-0052021-02-05
05391529585112ApexE03-010E03-0102021-02-05
05391529585129ApexE03-015E03-0152021-02-05
05391529585136ApexLE03-000LE03-0002021-02-05
05391529580773ApexE01-0052019-10-01
05391529580780ApexE01-0102019-10-01
05391529580797ApexE01-0152019-10-01

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