FDA.reportPublic FDA data

LiNA SeaStar™

Primary DI
05708265017300
Brand
LiNA SeaStar™
Company
LiNA Medical AG
Model
4000-S-Q
Device description
Single use retractor ring, Squared model
Published
2026-04-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GADRetractor

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GADRetractorGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
05708265017317PackageGS15In Commercial Distribution
05708265017300PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
05708265017317057082650173175708265017317
05708265017300057082650173005708265017300

GMDN Terms#

Term, Definition table
TermDefinition
Surgical retraction system mounting frame, single-useA noninvasive mounting device (e.g., a large ring, table-fixed bridging bar) designed as a component of a surgical retraction system, intended to be placed/fixed around a surgical incision site and upon which retraction system blades/components are mounted to temporarily part tissue (e.g., hold the edges of an incision open) to expose internal tissues or organs for access during surgery. It does not include the invasive retraction blades/components (i.e., is not the complete system). This is a single-use device.

Regulatory Flags#

DUNS number
485705870
Device count
1
Premarket exempt
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
05708265015306Drain Guard81502026-04-02
05708265015337EpiGuard81702026-04-02
05708265015368Pleura-Guard81612026-04-03
05708265015566LiNA PowerBlade™ 5005-E2026-04-03
05708265015627LiNA PowerBlade™ 5005-E-C2026-04-03
05708265015658LiNA PowerBlade™ 5005-E-C-1602026-04-03
05708265015801LiNA PowerBlade™ 5010-E2026-04-03
05708265015832LiNA PowerBlade™ 5010-E-1602026-04-03
05708265017201LiNA Skin Hook™SH-1102026-04-03
05708265017225LiNA Skin Hook™SH-1202026-04-03
05708265017249LiNA Skin Hook™SH-1302026-04-03
05708265017263LiNA Skin Hook™SH-2202026-04-03
05708265017324LiNA SeaStar™4000-S-SL2026-04-03
05708265017348LiNA SeaStar™4000-S-SS2026-04-03
05708265017362LiNA SeaStar™4000-S-VL2026-04-03
05708265017386LiNA SeaStar™4000-S-VS2026-04-03
05708265017409LiNA SeaStar™4000-S-VV2026-04-03
05708265017706LiNA OperaScope™ Biopsy ForcepsOP-FCP-62026-04-03
05708265017744LiNA OperaScope™ Rat Tooth Alligator GrasperOP-GRA-62026-04-03
05708265017881LiNA OperaScope™ Lasso OP-LAS10-32026-04-03

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00724995266912Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995266943Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995266950Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
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00724995266974Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995266981Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995266998Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995267001Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995267025Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995267032Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
00724995267537Snowden-PencerSTERIS Deutschland GmbHGAD2026-09-24
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