FDA.reportPublic FDA data

CAMLOG

Primary DI
00842092162880
Brand
CAMLOG
Company
Implants and Attachments, Inc.
Model
8003535
Catalog number
8003535
Device description
CAMLOG Screw-Line 5.0mm Non-Engaging Verification Cylinder
Published
2022-10-24
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
NDPAccessories, Implant, Dental, Endosseous
NHAAbutment, implant, dental, endosseous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NDPAccessories, Implant, Dental, EndosseousDental1
NHAAbutment, Implant, Dental, EndosseousDental2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00842092162880PackageGS110In Commercial Distribution
00842092103296PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00842092162880008420921628808420921628800842092162880
00842092103296008420921032968420921032960842092103296

GMDN Terms#

Term, Definition table
TermDefinition
Dental implant suprastructure, temporary, preformed, single-useA prefabricated device intended to be used during dental implant restorative and laboratory procedures to provide a temporary intermediate fixture level between a dental implant and a temporary dental prosthesis/restoration, during the oral soft-tissue healing and sculpturing period, prior to the fabrication/rehabilitation and installation of the final prosthesis/restoration (e.g., bridge, single tooth, overdenture). It typically includes burnout/temporary cylinders, fixture impression pick-ups, replica devices, caps/cover screws in a variety of shapes, sizes, and materials [e.g., titanium (Ti), plastic]. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(800) 232-7732lauren@preat.com
+1(800) 232-7732info@preat.com

Regulatory Flags#

DUNS number
054875224
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
00842092101063NobelBiocare™ Tri-Lobe-compatible 800055180005512023-08-10
00842092177105Preat Implant Prosthetics900373290037322022-11-03
00842092161708Preat Implant Prosthetics900475090047502022-11-03
00842092161784Preat Implant Prosthetics900703090070302022-11-03
00842092161814Preat Implant Prosthetics900723090072302022-11-03
00842092161845Preat Implant Prosthetics900703590070352022-11-03
00842092161876Preat Implant Prosthetics900723590072352022-11-03
00842092157169Preat Implant Prosthetics900643090064302022-10-31
00842092157213Preat Implant Prosthetics900653090065302022-10-31
00842092159132Preat Implant Prosthetics900665090066502022-10-31
00842092157268Preat Implant Prosthetics900663090066302022-10-31
00842092159149Preat Implant Prosthetics900675090067502022-10-31
00842092157312Preat Implant Prosthetics900673090067302022-10-31
00842092157350Preat Implant Prosthetics900683090068302022-10-31
00842092157381Preat Implant Prosthetics900643590064352022-10-31
00842092157411Preat Implant Prosthetics900653590065352022-10-31
00842092157442Preat Implant Prosthetics900663590066352022-10-31
00842092157473Preat Implant Prosthetics900673590067352022-10-31
00842092157503Preat Implant Prosthetics900683590068352022-10-31
00842092159576Preat Implant Prosthetics900583090058302022-11-01

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