FDA.reportPublic FDA data

ACUMED

Primary DI
10806378091001
Brand
ACUMED
Company
Acumed LLC
Model
80-2210
Device description
5.5mm PEEK SA Tap
Published
2015-10-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MBIFASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MBIFastener, Fixation, Nondegradable, Soft TissueOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K112111000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K112111000ACU-SINCH REPAIR SYSTEM AND ACUMED SUTURE ANCHORAcumed, LLC2011-11-14HTN

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10806378091001PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1080637809100110806378091001

GMDN Terms#

Term, Definition table
TermDefinition
Bone tap, reusableA metal surgical instrument designed for cutting internal threads into bone so that the threads facilitate the insertion of bone screws. The screws anchor bone fragments, fixtures and/or other devices to the bone. It is made of high-grade stainless steel and has a helical thread intersected with longitudinal cutting grooves forming the cutting edges at its distal end and may be cannulated. The proximal end typically terminates in a square to which a tapping instrument or extension can be attached. It will typically be manually rotated in order to create a best possible thread. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(888)627-9957businessservices@acumed.net

Regulatory Flags#

DUNS number
196884852
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10806378125997ACUMED3070-270082025-12-08
10806378126000ACUMED3070-270092025-12-08
10806378126017ACUMED3070-270102025-12-08
10806378126024ACUMED3070-270112025-12-08
10806378126031ACUMED3070-270122025-12-08
10806378126048ACUMED3070-270132025-12-08
10806378126055ACUMED3070-270142025-12-08
10806378126062ACUMED3070-270152025-12-08
10806378126079ACUMED3070-270162025-12-08
10806378126086ACUMED3070-270172025-12-08
10806378126093ACUMED3070-270182025-12-08
10806378126109ACUMED3076-300102025-12-08
10806378126116ACUMED3076-300122025-12-08
10806378126123ACUMED3076-300142025-12-08
10806378116810ACUMED80-40572026-08-18
10806378116827ACUMED80-40582026-08-18
10806378116841ACUMED80-40602026-08-18
10806378116858ACUMED80-40612026-08-18
10806378067341ACUMEDFX-4000-S2015-10-24
10806378067372ACUMEDFX-4001-S2015-10-24

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00860016070004ICONN Revolution 6.5MM Knotless Suture AnchorICONN ORTHOPEDICS LLCMBI2026-07-16