FDA.reportPublic FDA data

OSSIOfiber® Compression Staple System

Primary DI
07290017630717
Brand
OSSIOfiber® Compression Staple System
Company
OSSIO LTD
Model
OF2062522S
Catalog number
OF2062522S
Device description
OSSIOfiber® Compression Staple System, 25 x 22 mmPackage contains: 1 Implant, and 1 Instrument pack.
Published
2022-12-25
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
OJHOrthopedic Tray

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OJHOrthopedic TrayGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07290017630717PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07290017630717072900176307177290017630717

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic surgical procedure kit, non-medicated, single-useA collection of various sterile orthopaedic surgical instruments, dressings, and other materials intended to be used to perform an orthopaedic surgical procedure, however the kit is not dedicated to orthopaedic implantation. It does not contain pharmaceuticals. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Do not expose product to temperatures greater than 47°C or 116°F
Special Storage Condition, Specify00Keep dry
Special Storage Condition, Specify00Store at a normal relative humidity
Storage Environment Temperature7 Degrees Celsius30 Degrees Celsius

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-833-781-7373customer_service@ossio.io

Regulatory Flags#

DUNS number
600505107
Device count
1
Kit
true
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07290019361190OSSIOfiber® Interference ScrewOF1167023SOF1167023S2026-05-13
07290017630946OSSIOfiber® Suture AnchorOF1035551SOF1035551S2023-09-14
07290017630601OSSIOfiber® Suture AnchorOF1034751SOF1034751S2022-06-06
07290017630618OSSIOfiber® Suture AnchorOF1034752SOF1034752S2022-06-06
07290017630625OSSIOfiber® Suture AnchorOF1034753SOF1034753S2022-06-06
07290017630632OSSIOfiber® Suture AnchorOF1034754SOF1034754S2022-06-06
07290017630649OSSIOfiber® Suture AnchorOF1034755SOF1034755S2022-06-06
07290017630571OSSIOfiber® Trimmable Fixation Nail System, CannulatedOF2054070S1OF2054070S2026-02-19
07290017630588OSSIOfiber® Threaded Trimmable Fixation NailOF1104570SOF1104570S2025-12-17
07290017630595OSSIOfiber® Threaded Trimmable Fixation Nail SystemOF2104530SOF2104530S2025-12-17
07290017630823OSSIOfiber® Compression ScrewOF1073534SOF1073534S2025-09-26
07290017630830OSSIOfiber® Compression ScrewOF1073536SOF1073536S2025-09-26
07290017630847OSSIOfiber® Compression ScrewOF1073538SOF1073538S2025-09-26
07290017630854OSSIOfiber® Compression ScrewOF1073540SOF1073540S2025-09-26
07290019361176OSSIOfiber® Suture AnchorOF1032554SOF1032554S2025-09-08
07290019361121OSSIO® Drill PackTHN00482THN004822024-10-07
07290019361138OSSIO® Drill PackTHN00483THN004832024-10-07
07290019361145OSSIO® Drill PackTHN00484THN004842024-10-07
07290019361152OSSIOfiber® Suture AnchorOF1032552SOF1032552S2025-05-29
07290019361169OSSIOfiber® Suture AnchorOF1032553SOF1032553S2025-05-29

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