FDA.reportPublic FDA data

4.2mm Parallel Pin

Primary DI
00810118210174
Brand
4.2mm Parallel Pin
Company
Osteocentric Technologies, Inc.
Model
701-0017
Catalog number
701-0017
Device description
4.2mm Parallel Pin
Published
2023-10-30
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
FZXGuide, Surgical, Instrument

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FZXGuide, Surgical, InstrumentGeneral, Plastic Surgery1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K230242000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K230242000OsteoCentric Dental Implant SystemOsteoCentric Technologies2023-10-05DZE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810118210174PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810118210174008101182101748101182101740810118210174

GMDN Terms#

Term, Definition table
TermDefinition
Dental implant systemA collection of devices designed for the surgical placement of a dental implant into alveolar and/ or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g., bridge, single-tooth, overdenture). It typically consists of a sterile endosteal dental implant (implant body and abutment) and surgical instruments for implantation.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
1-800-969-0639quality@osteocentric.com

Regulatory Flags#

DUNS number
089645059
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
008100978037493.0mm GUIDE WIRE 355mm202-80600202-806002026-06-02
00810118210198Torque Wrench701-0019701-00192023-10-31
00810118210259.050 Driver, Short701-0025701-00252023-10-31
00810118210266.050 Driver, Long701-0026701-00262023-10-31
00810118210273.050 Driver, Latch701-0027701-00272023-10-31
00810118210280Thumb Knob701-0029701-00292023-10-31
00810118210327Latch Driver, 300 Series701-0033701-00332023-10-31
00810118210334Square Driver, 300 Series701-0034701-00342023-10-31
00810118210341Latch Driver, 400 Series701-0035701-00352023-10-31
00810118210358Square Driver, 400 Series701-0036701-00362023-10-31
00810118210365Ratchet Adapter701-0037701-00372023-10-31
008101182100063.7mm Tap701-0013701-00132023-10-30
008101182100134.2mm Tap701-0014701-00142023-10-30
008101182100205.5mm Tap701-0015701-00152023-10-30
00810118210129Drill Extender701-0009701-00092023-10-30
008101182101673.7mm Parallel Pin701-0016701-00162023-10-30
008101182101815.5mm Parallel Pin701-0018701-00182023-10-30
00810097803527NAV 3.5mm DRILL104-0003104-00032026-03-26
00810097803534NAV TAPERED PROBE104-0005104-00052026-03-26
00810097803541NAV SOLID TAP FOR 5.5mm FASTENER104-0112104-01122026-03-26

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190776423896MillenniumAvalign Technologies, Inc.FZX2026-08-26
10886982362988NASynthes GmbHFZX2026-08-26
10886982362995NASynthes GmbHFZX2026-08-26
10886982363008NASynthes GmbHFZX2026-08-26
10886982363015NASynthes GmbHFZX2026-08-26
008890247114712.9 JuggerKnot Self-Punching ObturatorZimmer, Inc.FZX2026-08-25
008890247114882.9 JuggerKnot Self-Punching CannulaZimmer, Inc.FZX2026-08-25
00889024712294Pin Target AssemblyZimmer, Inc.FZX2026-08-25
06937278653598CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278653604CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278653611CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278653628CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654250CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654267CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654281CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654304CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654748CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654755CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654762CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654779CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654786CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654823CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654830CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654847CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654854CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654861CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654878CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654885CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654892CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22
06937278654908CurawayZhejiang CuraWay Medical Technology Co., Ltd.FZX2026-08-22