FDA.reportPublic FDA data

Arthrex®

Primary DI
10888867225388
Brand
Arthrex®
Company
ARTHREX, INC.
Model
ABS-4056
Catalog number
ABS-4056
Device description
4.0" DIAMETER HELIX COMPOSITE LAYER
Published
2017-02-15
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FRODressing, wound, drug

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FRODressing, Wound, DrugUnknownU

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K130350000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K130350000PROCELLERAVomaris Innovations, Inc.2013-07-02FRO

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10888867225388PrimaryGS10
M150ABS40561SecondaryHIBCC0
00888867225381Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088886722538810888867225388
00888867225381008888672253818888672253810888867225381

GMDN Terms#

Term, Definition table
TermDefinition
Exudate-absorbent dressing, non-gel, antimicrobial, sterileA sterile wound covering intended to absorb exudates and blood from a wound (e.g., ulcers, burns, surgical wounds, lacerations, abrasions, and/or percutaneous device wounds), and that contains an antimicrobial agent [e.g., silver (Ag), chlorhexidine gluconate (CHG)]. It is not in the form of a gel and does not produce a water-absorbent gel upon contact with wound exudate. It is intended to create a moist wound-healing environment and/or protect wounds from external contamination by microorganisms from the periwound skin. The device may be in the form of a flat sheet/film, ribbon, rope, foam, liquid, or powder. After application, this device cannot be reused.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)934-4404complaints@arthrex.com

Regulatory Flags#

DUNS number
131747628
Device count
10
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
true
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
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 table
Primary DIBrandModelCatalogPublished
00888867498105Arthrex®AR-3210-0037AR-3210-00372026-07-31
00888867532236Arthrex®AR-S7500-030-260-SAR-S7500-030-260-S2026-07-31
00888867532243Arthrex®AR-S7500-030-360-SAR-S7500-030-360-S2026-07-31
00888867532250Arthrex®AR-S7500-040-260-SAR-S7500-040-260-S2026-07-31
00888867532267Arthrex®AR-S7500-040-360-SAR-S7500-040-360-S2026-07-31
00888867532274Arthrex®AR-S7500-050-260-SAR-S7500-050-260-S2026-07-31
00888867544819Arthrex®AR-S7510-030-260AR-S7510-030-2602026-07-31
00888867544826Arthrex®AR-S7510-040-260AR-S7510-040-2602026-07-31
00888867544833Arthrex®AR-S7510-050-260AR-S7510-050-2602026-07-31
00888867544840Arthrex®AR-S7563-030-260AR-S7563-030-2602026-07-31
00888867544857Arthrex®AR-S7563-030-360AR-S7563-030-3602026-07-31
00888867544864Arthrex®AR-S7570-030-260AR-S7570-030-2602026-07-31
00888867544871Arthrex®AR-S7570-030-360AR-S7570-030-3602026-07-31
00888867544888Arthrex®AR-S7570-040-260AR-S7570-040-2602026-07-31
00888867544895Arthrex®AR-S7570-040-360AR-S7570-040-3602026-07-31
00888867572010Arthrex®AR-S7500-000-000WAR-S7500-000-000W2026-07-31
00888867572034Arthrex®AR-S7500-100-000WAR-S7500-100-000W2026-07-31
00888867572041Arthrex®AR-S7500-100-000FAR-S7500-100-000F2026-07-31
00888867571129Arthrex®ABS-1981-20SABS-1981-20S2026-07-29
00888867020498Arthrex®AR-1648AR-16482018-08-03

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00818582013796Puracyn® Plus Professional FormulaInnovacyn, Inc.FRO2026-07-31
00818582013802Puracyn® Plus Professional FormulaInnovacyn, Inc.FRO2026-07-31
10197344169405MEDLINEMEDLINE INDUSTRIES, INC.FRO2026-07-31
00852421007683Pure&CleanPure & Clean, LLCFRO2026-07-29
00852421007850Pure&CleanPure & Clean, LLCFRO2026-07-29
04260056880667XPERIENCE Advanced Surgical IrrigationOSARTIS GmbHFRO2026-07-28
10841495149815QUIKCLOTTELEFLEX INCORPORATEDFRO2026-07-27
B665AC510011AC5 Advanced Wound SystemArch Therapeutics, Inc.FRO2026-07-24
B665AVX030011VIA LinxArch Therapeutics, Inc.FRO2026-07-24
00852421007300Pure&CleanPure & Clean, LLCFRO2026-07-22
00818582012867Puracyn® Plus OTCInnovacyn, Inc.FRO2026-07-17
00818582012881Puracyn® Plus OTCInnovacyn, Inc.FRO2026-07-17
00852009002451Puracyn® Plus OTCInnovacyn, Inc.FRO2026-07-17
00852009002475Puracyn® Plus OTCInnovacyn, Inc.FRO2026-07-17
00852009002536Puracyn® Plus OTCInnovacyn, Inc.FRO2026-07-17
10197344169450MEDLINEMEDLINE INDUSTRIES, INC.FRO2026-07-17
09551012610479ELECTROCYN somaV3BIO SDN. BHD.FRO2026-07-16
10197344176007MEDLINEMEDLINE INDUSTRIES, INC.FRO2026-07-13
10197344176014MEDLINEMEDLINE INDUSTRIES, INC.FRO2026-07-13
10197344176021MEDLINEMEDLINE INDUSTRIES, INC.FRO2026-07-13
10197344176038MEDLINEMEDLINE INDUSTRIES, INC.FRO2026-07-13
04260056880650BLASTXOSARTIS GmbHFRO2026-07-12
00850088144604CARBOUNingbo kehu Medical Technology Co.,Ltd.FRO2026-07-10
00850088144611CARBOUNingbo kehu Medical Technology Co.,Ltd.FRO2026-07-10
00850088144628CARBOUNingbo kehu Medical Technology Co.,Ltd.FRO2026-07-10
00850088144635CARBOUNingbo kehu Medical Technology Co.,Ltd.FRO2026-07-10
00850019138146SilverSealNEXGEL Inc.FRO2026-07-08
00850019138153TurfGuardNEXGEL Inc.FRO2026-07-08
00850019138443SilverSealNEXGEL Inc.FRO2026-07-08
00850019138474SilverSealNEXGEL Inc.FRO2026-07-08