FDA.reportPublic FDA data

CeraRoot Implant System

Primary DI
08435453900508
Brand
CeraRoot Implant System
Company
CERAROOT SL.
Model
005.114
Catalog number
005.114
Device description
Surgical Mallet. Both ends of the head are covered by Teflon caps that are autoclavable. Length of the head is 2.5 inches. Length of the handle is 6.5 inches
Published
2019-09-15
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
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
DZNInstruments, Dental Hand

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DZNInstruments, Dental HandDental1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K093595000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K093595000CERAROOT IMPLANT SYSTEMOral Iceberg S.L.2011-01-04DZE

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08435453900508PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08435453900508084354539005088435453900508

GMDN Terms#

Term, Definition table
TermDefinition
Surgical malletA hand-held manual surgical instrument designed to strike a surface or another device (e.g., a surgical chisel, gouge, driver) to drive it during a surgical intervention. It is available in a variety of designs and materials; the shaft is typically made of metal (e.g., chromed iron (Fe) or high-grade stainless steel), but can be made of synthetic materials (e.g., Tufnol), and tapers distally to the head. The head is typically a solid, cylindrical shape normally being double-ended and made of solid (iron/steel) or shock-absorbing materials (e.g., rubber, plastic, or Tufnol). Also referred to as a surgical hammer it may also be used for autopsy. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+34937683962info@ceraroot.com

Regulatory Flags#

DUNS number
467001948
Device count
1
DM exempt
true
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
08435453901116CeraRoot® Implant 16TL, L 8162.008162.0082026-09-22
08435453901123CeraRoot® Implant 16TL, L 10162.010162.0102026-09-22
08435453901130Implant CeraRoot 16TL:12/4.8-6.5162.012162.0122026-09-22
08435453901154CeraRoot® Implant 21TL, L 8212.008212.0082026-09-22
08435453901161CeraRoot® Implant 21TL, L 10212.010212.0102026-09-22
08435453901178CeraRoot® Implant 21TL, L 12212.012212.0122026-09-22
08435453901192CeraRoot® Implant 34TL, L 8342.008342.0082026-09-22
08435453901208CeraRoot® Implant 34TL, L 10342.010342.0102026-09-22
08435453901215CeraRoot® Implant 34TL, L 12342.012342.0122026-09-22
08435453901321CeraRoot® Implant 16TL, L 14162.014162.0142026-09-22
08435453901338CeraRoot® Implant 21TL, L 14212.014212.0142026-09-22
08435453901345CeraRoot® Implant 34TL, L 14342.014342.0142026-09-22
08435453901352Abutment 16TL - 4mm162.104162.1042026-09-22
08435453901369Abutment 16TL - 6mm162.106162.1062026-09-22
08435453901376Abutment 34TL - 4mm342.104342.1042026-09-22
08435453901383Abutment 34TL -6mm342.106342.1062026-09-22
08435453901512Abutment 21TL - 4mm212.104212.1042026-09-22
08435453901529Abutment 21TL -6mm212.106212.1062026-09-22
08435453900515CeraRoot Implant System005.214005.2142019-09-15
08435453901086CeraRoot Implant System006.111006.1112025-04-27

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10860013564770CurvaGc Orthodontics America Inc.DZN2026-05-28
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