Awl 285943

GUDID 00811714036311

5.5 mm Reusable Awl

RESPONSIVE ORTHOPEDICS LLC

Bone awl, reusable
Primary Device ID00811714036311
NIH Device Record Key1b736171-0cd4-4c8f-8e8e-30b3846a3835
Commercial Distribution StatusIn Commercial Distribution
Brand NameAwl
Version Model Number285943
Catalog Number285943
Company DUNS002745858
Company NameRESPONSIVE ORTHOPEDICS LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100811714036311 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


[00811714036311]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-22
Device Publish Date2025-05-14

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00811714034362Awl
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008117140363115.5 mm Reusable Awl
00811714036304Awl

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