FDA.reportPublic FDA data

FlexBand Plus

Primary DI
00850003396071
Brand
FlexBand Plus
Company
Artelon
Model
41053
Catalog number
41053
Published
2019-12-27
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

Product Codes#

Code, Name table
CodeName
FTLMesh, Surgical, Polymeric
MBIFastener, Fixation, Nondegradable, Soft Tissue
QWJMesh, Surgical, Polymeric, Resorbable, Orthopedics, Reinforcement Of Ligament

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FTLMesh, Surgical, PolymericGeneral, Plastic Surgery2
MBIFastener, Fixation, Nondegradable, Soft TissueOrthopedic2
QWJMesh, Surgical, Polymeric, Resorbable, Orthopedics, Reinforcement Of LigamentGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K192112000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K192112000FlexBand PlusInternational Life Sciences2019-09-27FTL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850003396071PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850003396071008500033960718500033960710850003396071

GMDN Terms#

Term, Definition table
TermDefinition
Polyester suture, bioabsorbable, monofilamentA single-strand (monofilament), synthetic, bioabsorbable thread made from a polyester (e.g., polydioxanone, poliglecaprone, polycaprolactone, polyglyconate, polyhydroxybutyrate) intended to join (approximate) the edges of a soft-tissue wound or incision by stitching or to ligate soft tissues. The thread provides extended temporary wound support, until the wound sufficiently heals to withstand normal stress, and is subsequently absorbed by hydrolysis; it may include an attached disposable needle. It is not a barbed suture and does not include antimicrobial agents/materials. This is a single-use device intended to be used in a sterile condition.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Length8Centimeter
Width0.5Centimeter

Sterilization Methods#

Method table
Method
Ethylene Oxide;Radiation Sterilization

Regulatory Flags#

DUNS number
066284070
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850003396217FLEXBAND FIX51013510132023-05-24
00850003396248FlexBandTW012TW0122024-04-11
00850003396323FlexBandTW030TW0302024-04-11
00850003396187FlexBand Plus41068410682023-05-24
00850003396286FlexBand71004710042023-05-24
00850003396163FlexBand71016710162021-02-25
00850003396170FlexBand51004510042021-02-25
00868047000304FlexPatch31048310482019-12-23
00868047000311FlexPatch31050310502019-12-23
00868047000328FlexPatch31049310492019-12-23
00868047000335FlexBand31051310512019-12-23
00868047000342FlexBand31052310522019-12-23
00868047000359FlexBand31053310532019-12-23
00868047000366FlexBand31054310542019-12-23
00868047000373FlexBand31055310552019-12-23
00868047000380FlexBand31056310562019-12-23
00868047000397FlexBand31058310582019-12-23
00850003396033FlexBand Plus41057410572019-12-27
00850003396040FlexBand Plus41056410562019-12-27
00850003396057FlexBand Plus41055410552019-12-27

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Primary DI, Brand, Company table
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20845854655501Argo KnotlessConmed CorporationMBI2026-09-25
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00889024711280Jgrknt Reusable Fishmouth Perc GuideBiomet Orthopedics, LLCMBI2026-08-25
00889024712034Percutaneous Soft Anchor Short 1.4mm GuideBiomet Orthopedics, LLCMBI2026-08-25
00810198920178TeKBraceTheraMicro, LLCMBI2026-08-14
00811714036472ThunderboltRESPONSIVE ORTHOPEDICS LLCMBI2026-07-31
00811714036489ThunderboltRESPONSIVE ORTHOPEDICS LLCMBI2026-07-31
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