92-02324

GUDID 07613327682724

Pediatr. mandib. distractor 25mm left

Stryker Leibinger GmbH & Co. KG

Implantable craniofacial bone distractor
Primary Device ID07613327682724
NIH Device Record Key36117c8b-a6aa-4693-a82b-824f9ed6811f
Commercial Distribution StatusIn Commercial Distribution
Version Model Number92-02324
Catalog Number92-02324
Company DUNS316153956
Company NameStryker Leibinger GmbH & Co. KG
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter
Width26.2 Millimeter
Device Size Text, specify0
Height4.3 Millimeter
Length57.8 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327682724 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQNEXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-09
Device Publish Date2026-02-27

Devices Manufactured by Stryker Leibinger GmbH & Co. KG

07613327682717 - NA2026-03-09 Pediatr. mandib. distractor 25mm right
07613327682724 - NA2026-03-09Pediatr. mandib. distractor 25mm left
07613327682724 - NA2026-03-09 Pediatr. mandib. distractor 25mm left
37613327090810 - NA2026-02-18 Screws, increased head, Cross-Pin
37613327090827 - NA2026-02-18 Screws, increased head, Cross-Pin
37613327090834 - NA2026-02-18 Screws, increased head, Cross-Pin
37613327090841 - NA2026-02-18 Screws, increased head, Cross-Pin
37613327090858 - NA2026-02-18 Bone Screws, square-fit, self-tapping
37613327090865 - NA2026-02-18 Bone Screws, square-fit, self-tapping

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