DUALX DUAL PORTAL PITUITARY STRAIGHT 2.0mm

GUDID B7076020030

PITUITARY STRAIGHT 2.0mm

Amplify Surgical, Inc.

Orthopaedic implant inserter/extractor, reusable
Primary Device IDB7076020030
NIH Device Record Keye1551f29-05ef-49fb-9edc-0402d7d6673b
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUALX DUAL PORTAL PITUITARY STRAIGHT 2.0mm
Version Model Number602003
Company DUNS081021000
Company NameAmplify Surgical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB7076020030 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


[B7076020030]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-28
Device Publish Date2022-11-18

Devices Manufactured by Amplify Surgical, Inc.

B707125355740300 - DUALX DUAL PORTAL DISPOSABLE KIT-30MM (USA)2026-03-13 INCLUDES: CANNULA 30MM HEMOSTATIC AGENT DELIVERY TUBE
B707125355740400 - DUALX DUAL PORTAL DISPOSABLE KIT-40MM (USA)2026-03-13 INCLUDES: CANNULA 40MM HEMOSTATIC AGENT DELIVERY TUBE
B707125355740500 - DUALX DUAL PORTAL DISPOSABLE KIT-50MM (USA)2026-03-13 INCLUDES: CANNULA 50MM HEMOSTATIC AGENT DELIVERY TUBE
B707125355740600 - DUALX DUAL PORTAL DISPOSABLE KIT-60MM (USA)2026-03-13 INCLUDES: CANNULA 60MM HEMOSTATIC AGENT DELIVERY TUBE
B707125355740700 - DUALX DUAL PORTAL DISPOSABLE KIT-70MM (USA)2026-03-13 INCLUDES: CANNULA 70MM HEMOSTATIC AGENT DELIVERY TUBE
B707125355740800 - DUALX DUAL PORTAL DISPOSABLE KIT-80MM (USA)2026-03-13 INCLUDES: CANNULA 80MM HEMOSTATIC AGENT DELIVERY TUBE
B707125355740900 - DUALX DUAL PORTAL DISPOSABLE KIT-90MM (USA)2026-03-13 INCLUDES: CANNULA 90MM HEMOSTATIC AGENT DELIVERY TUBE
B707125355741000 - DUALX DUAL PORTAL DISPOSABLE KIT-100MM (USA)2026-03-13 INCLUDES: CANNULA 100MM HEMOSTATIC AGENT DELIVERY TUBE

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