FDA.reportPublic FDA data

Omnia Medical TiBrid™-A

Primary DI
00843511113155
Brand
Omnia Medical TiBrid™-A
Company
OMNIA MEDICAL, LLC
Model
14-5A-INS2
Catalog number
14-5A-INS2
Device description
ALIF Inserter, 45°
Published
2025-03-14
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
MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K190363000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K190363000Omnia Medical TiBrid Cervical Cage, Omnia Medical TiBrid Lateral Cage, Omnia Medical TiBrid ALIF Cage, Omnia Medical TiBrid PLIF Cage, Omnia Medical TiBrid TLIF CageOmnia Medical, LLC2020-02-21MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00843511113155PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00843511113155008435111131558435111131550843511113155

GMDN Terms#

Term, Definition table
TermDefinition
Surgical implant/trial-implant/sizer holder, reusableA hand-held manual surgical instrument designed to connect to and hold an implant (e.g., bone screw, bone graft), trial implant, or implantable device sizer/template (e.g., glenoid defect sizer, hearing implant template) to facilitate guidance, gauging/sizing, and/or monitoring of the held device during orthopaedic or ear/nose/throat (ENT) surgery. The instrument is typically made of metal or synthetic polymer materials and is typically constructed in the form of a long shaft with a handle at the proximal end and a device holding/fixation mechanism at the distal end. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
3044134851customerservice@omniamedical.com

Regulatory Flags#

DUNS number
079467378
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00843511128777Omnia Medical TiBrid™-A/SA14-5A-QAT114-5A-QAT12026-06-01
00843511128388Omnia Medical TiBrid™- A/SA 17-5A-BL0617-5A-BL062026-05-11
00843511128395Omnia Medical TiBrid™- A/SA 17-5A-BL082026-05-11
00843511128401Omnia Medical TiBrid™- A/SA 17-5A-BL102026-05-11
00843511128418Omnia Medical TiBrid™- A/SA 17-5A-BL122026-05-11
00843511128425Omnia Medical TiBrid™- A/SA 17-5A-BL142026-05-11
00843511128432Omnia Medical TiBrid™- A/SA 17-5A-BL162026-05-11
00843511128463Omnia Medical TiBrid™- A/SA 17-5A-AWL1-B2026-05-11
00843511128494Omnia Medical TiBrid™-C07-5C-LTDE2026-05-11
00843511128500Omnia Medical Instruments99-5A-CL132026-05-11
00843511128517Omnia Medical Instruments99-5A-CL202026-05-11
00843511128548Omnia Medical Golden Spike OM-TLS4015-T2026-05-11
00843511128555Omnia Medical Golden Spike OM-TLS4016-T2026-05-11
00843511128562Omnia Medical Golden Spike OM-TLS4017-T2026-05-11
00843511128579Omnia Medical Golden Spike OM-TLS4018-T2026-05-11
00843511128586Omnia Medical Golden Spike OM-TLS4019-T2026-05-11
00843511128593Omnia Medical Golden Spike OM-TLS4020-T2026-05-11
00843511128609Omnia Medical Golden Spike OM-TLS4021-T2026-05-11
00843511128616Omnia Medical Golden Spike OM-TLS4022-T2026-05-11
00843511128623Omnia Medical Golden Spike OM-TLS4023-T2026-05-11

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08800043912870N/ATDM Co., Ltd.MAX2026-06-02
08800043912887N/ATDM Co., Ltd.MAX2026-06-02
08800043912894N/ATDM Co., Ltd.MAX2026-06-02
08800043912900N/ATDM Co., Ltd.MAX2026-06-02
08800043912917N/ATDM Co., Ltd.MAX2026-06-02
08800043912924N/ATDM Co., Ltd.MAX2026-06-02
08800043912931N/ATDM Co., Ltd.MAX2026-06-02
08800043912948N/ATDM Co., Ltd.MAX2026-06-02
08800043912955N/ATDM Co., Ltd.MAX2026-06-02
08800043912962N/ATDM Co., Ltd.MAX2026-06-02
08800043912979N/ATDM Co., Ltd.MAX2026-06-02
08800043912986N/ATDM Co., Ltd.MAX2026-06-02
08800043912993N/ATDM Co., Ltd.MAX2026-06-02
08800043913006N/ATDM Co., Ltd.MAX2026-06-02
08800043913013N/ATDM Co., Ltd.MAX2026-06-02
08800043913020N/ATDM Co., Ltd.MAX2026-06-02
08800043913037N/ATDM Co., Ltd.MAX2026-06-02
08800043913044N/ATDM Co., Ltd.MAX2026-06-02
08800043913051N/ATDM Co., Ltd.MAX2026-06-02
08800043913068N/ATDM Co., Ltd.MAX2026-06-02
08800043913075N/ATDM Co., Ltd.MAX2026-06-02
08800043964183N/ATDM Co., Ltd.MAX2026-06-02
08800043964190N/ATDM Co., Ltd.MAX2026-06-02
08800043964206N/ATDM Co., Ltd.MAX2026-06-02
08800043964213N/ATDM Co., Ltd.MAX2026-06-02
08800043964220N/ATDM Co., Ltd.MAX2026-06-02
08800043964237N/ATDM Co., Ltd.MAX2026-06-02
08800043964244N/ATDM Co., Ltd.MAX2026-06-02
08800043964251N/ATDM Co., Ltd.MAX2026-06-02
08800043964268N/ATDM Co., Ltd.MAX2026-06-02