FDA.reportPublic FDA data

Implant Prosthetics

Primary DI
00842092165997
Brand
Implant Prosthetics
Company
PREAT CORPORATION
Model
9001435
Catalog number
9001435
Device description
Straumann Bone Level RC Non-Engaging Verification Cylinder Kit contains: 1 Straumann Bone Level RC Non-Engaging Verification Cylinder (00842092125915) 1 Straumann Bone Level RC Guide Pin 20mm (00842092133774) 1 Straumann Bone Level RC Titanium Screw (00842092165959)
Published
2022-09-06
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
NHAAbutment, Implant, Dental, Endosseous

Product Code Classifications#

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

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00842092166000PackageGS110In Commercial Distribution
00842092165997PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00842092166000008420921660008420921660000842092166000
00842092165997008420921659978420921659970842092165997

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

Regulatory Flags#

DUNS number
054875224
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
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
00842092187647Equator214290121429012026-02-25
00842092187654Equator214290221429022026-02-25
00842092186640Equator214299221429922026-02-06
00842092186657Equator214299621429962026-02-05
00842092186664Equator214200321420032026-02-05
00842092184028Preat7101067101062025-12-22
00842092184073Preat7100457100452025-12-22
00842092184080Preat7100467100462025-12-22
00842092184134Preat7100557100552025-12-22
00842092184141Preat7100567100562025-12-22
00842092184301Preat7100107100102025-12-22
00842092184370Preat7100207100202025-12-22
00842092184660Preat7100857100852025-12-22
00842092184677Preat7100867100862025-12-22
00842092184721Preat7100957100952025-12-22
00842092184738Preat7100967100962025-12-22
00842092184745Preat7101517101512025-12-22
00842092184783Preat7101557101552025-12-22
00842092184790Preat7101567101562025-12-22
00842092184844Preat7101457101452025-12-22

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00840481138218LOCATOR FixedZest Anchors, LLCNHA2026-05-22
00840481138225LOCATOR FixedZest Anchors, LLCNHA2026-05-22
00840481138232LOCATOR FixedZest Anchors, LLCNHA2026-05-22
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