Packaging systems for dental implants and methods for implanting a packaged implant are provided herein. The packaging system includes a housing and a cap forming an enclosure for a dental implant and corresponding healing screw. The housing includes a first and second base portion that interact with a platform that receives a portion of the dental implant to present the dental implant to a user during use.

A process for the preparation of a topography for improved fibrin network formation and cell mineralization on at least a portion of a dental implant made of a binary titanium-zirconium alloy, the portion being destined to be embedded in a patient's jawbone and to be in contact with the jawbone via a bone-contacting surface, the process includes the subsequent steps of a) subjecting the bone-contacting surface of the dental implant to a sandblasting treatment, b) etching the sandblasted bone-contacting surface, and c) treating the sandblasted and etched bone-contacting surface with water or an aqueous solution for a duration of more than two days, during which nanostructures continuously grow on the bone-contacting surface, the nanostructures extending in at least two dimensions to 200 nm at most. The process is characterized in that the treatment of b) is carried out at a temperature from 40 C. to 60 C.

The present invention relates to packaging and in particular, to sterile packaging that is configured to be self-stackable and interlocking. A sterile packaging comprising a packaging compartment provided having one open face through which the compartment may be filled, the open face forms a sterile sealing face that is to be sealed with and receive a sterile barrier. The package features at least one coupling interface along an external surface having male to female couplers configured to facilitate piggy-back coupling between two packaging.

A dental protocol for creating an osteotomy for an implant is disclosed. A first drill is selected having a tip to create a pilot hole in the bone surface of a patient. The first drill includes a first boring section to create a bore hole for a second drill and a second boring section to create a coronal area on the hole near the bone surface. A first drill hole is created on the bone surface having a depth compatible with the length of the implant with the first drill and a coronal area. A second drill for creating a second hole having a width compatible with the body of the implant is selected. A second drill hole is created on the bone surface with the second drill.

The invention relates to a bioinert body having a base body, which grows to a multiple of its volume when hydrated. The base body substantially consists of dried laminaria parts, which also develop a local antibacterial effect due to the iodine content. The bioinert body is suitable for application in a method of tissue augmentation.

The present disclosure relates to an implant surface modification treatment device including an internal electrode having a barrel-shaped structure and a surface on which a plurality of transmission parts are formed, an ultraviolet (UV) discharge vessel having a barrel-shaped structure that accommodates the internal electrode and has a gas-filled area filled with a discharge gas that serves as a UV light source, and an external electrode accommodating the UV discharge vessel inside thereof, wherein an implant fixture is placed inside the internal electrode to perform surface modification.

An implant storage container according to an embodiment of present invention comprises an implant body, a holding block connected to the implant body, a cover storing the implant body and connected to the holding block and a sealing member configured to seal a boundary between the holding block and the cover to maintain a vacuum state inside the cover.

A dental implant made of a ceramic material including an implant surface having at least partially a contact angle of less than 20, the implant surface being at least partially covered by a protective layer. The protective layer includes a dextran having a molecular weight of more than 15,000 Da.

A partially customizable single-piece dental implant includes a preformed bone-anchorage component and an abutment component that is custom milled from a block either preoperatively, (i.e., Process A) or intraoperatively, (i.e., Process B). In Process A, the planned abutment shape is designed by a computer-aided design (CAD) software based on a computerized tomographic scan and other patient data. Alternatively, under Process B, the position of the planned implant with respect to the alveolus is digitally captured (e.g., by an optical impression device or an intraoperative computerized tomographic scan). In both Process A and Process B, a blank implant having the millable block is held to allow a computer-aided manufacturing (CAM) machine to customize the abutment component, as well as part of the bone-anchorage component. The resultant dental implant is then inserted in the alveolus and either a provisional or permanent prosthesis can then be immediately loaded on the implant.

Disclosed herein are elastic, bioresorbable encasements for medical implants, methods for making the same and uses thereof.