REVCON

Primary DI
00850041704074
Brand
REVCON
Company
Voom Medical Devices, Inc
Model
VDG01000
Catalog number
VDG01000
Device description
Depth Gauge
Published
2023-04-05
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
HWCScrew, Fixation, Bone

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HWCScrew, Fixation, BoneOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K223392000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K223392000REVCON (TM) Screw SystemVoom Medical Devices, Inc.2023-02-28HWC

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850041704074PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850041704074008500417040748500417040740850041704074

GMDN Terms#

Term, Definition table
TermDefinition
Surgical depth gauge, reusableA surgical instrument designed to measure the depth of a recess, usually to measure the depth of holes being drilled in bone so that the surgeon can determine the length of the bone screw to be used. It may take two forms: 1) a device with a moveable (sliding) centrepiece (a prong), the tip of which is inserted into the recess to read from a scale; 2) a circular disc with a central hole which is clipped to a drill bit so that the device slides up as the drill bit is advanced. This is a reusable device intended to be sterilized prior to use.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
844-372-5489info@voommedicaldevices.com

Regulatory Flags#

DUNS number
080898988
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
false
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
00850041704005REVCONVTR01000VTR010002023-04-05
00850041704036REVCONVKW01000VKW010002023-04-05
00850041704043REVCONVKW01001VKW010012023-04-05
00850041704050REVCONVEL01000VEL010002023-04-05
00850041704067REVCONVEL01001VEL010012023-04-05
00850041704081REVCONVDB01000VDB010002023-04-05
00850041704098REVCONVDB01001VDB010012023-04-05
00850041704104REVCONVDR01000VDR010002023-04-05
00850041704111REVCONVDR01001VDR010012023-04-05
00850041704128REVCONVHA01000VHA010002023-04-05
00850041704135REVCONVHA01001VHA010012023-04-05
00850041704142REVCONRSN3020RSN30202023-04-05
00850041704159REVCONRSN3022RSN30222023-04-05
00850041704166REVCONRSN3024RSN30242023-04-05
00850041704173REVCONRSN3026RSN30262023-04-05
00850041704180REVCONRSN3028RSN30282023-04-05
00850041704197REVCONRSN3030RSN30302023-04-05
00850041704203REVCONRSN3032RSN30322023-04-05
00850041704210REVCONRSN3034RSN30342023-04-05
00850041704227REVCONRSN3036RSN30362023-04-05

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Primary DI, Brand, Company table
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00810112592986TriLeap Lower Extremity Anatomic Plating SystemSynthes GmbHHWC2024-02-22
00810112592993TriLeap Lower Extremity Anatomic Plating SystemSynthes GmbHHWC2024-02-22
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00810112593099TriLeap Lower Extremity Anatomic Plating SystemSynthes GmbHHWC2024-02-22
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00810112593143TriLeap Lower Extremity Anatomic Plating SystemSynthes GmbHHWC2024-02-22
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