Dentium.

Dentium's U.S. about page says Dentium Co. Ltd. was founded in Seoul in June 2000 and that Dentium USA was founded in Cypress, California in February 2004. The same timeline says the Implantium system received U.S. FDA clearance in August 2004. The current footer on Dentium USA pages lists an office and manufacturing address at 6731 Katella Avenue, Cypress, CA 90630. A July 2010 entry records an East Coast branch in Englewood Cliffs, New Jersey. The company says it serves clinicians in more than 80 countries.

The implant index on Dentium USA lists four bone-level names: SuperLine II and SuperLine, both described for immediate loading, plus Implantium and NR Line. The SuperLine product page describes an SLA surface, unalloyed grade 4 titanium under ASTM F67, a single connection across diameters, and abutments the company says can be used on any diameter and across three of its implant systems. It also says those SuperLine implants are manufactured in the United States. The body is described as double-threaded and tapered, with three apical cutting flutes.

Regenerative products are on the same timeline, with dates a buyer can check. Osteon I was developed in 2005, received a CE certificate in 2006, and FDA clearance in 2007. Osteon II was developed in 2011 and received FDA clearance in 2012. A resorbable collagen membrane was developed in 2010 and received FDA clearance in 2011. Later entries include SimpleLine II and SlimLine FDA clearance in 2012, NR Line FDA clearance in 2016, SuperLine II FDA clearance in 2017, and a titanium-base custom abutment clearance in 2019. Use the clearance year as a history of the portfolio, then rely on the current indication for the SKU you order.

Dentium says the implants are backed by more than 20 years of clinical data and names university collaborators on the about page, including Loma Linda, the University of Michigan, and others. That is the company's description of its evidence file. This profile does not repeat marketing success-rate percentages from the same page. Education is offered as a study club and as seminars that the site says carry continuing-education credit.

For a U.S. practice, the buying path is Dentium USA in Cypress, not a guess that every component is machined there. The SuperLine page makes a U.S. manufacturing statement about that implant. Other lines should be confirmed on their own pages. Laboratory components are part of the about-page catalog, so the restoring lab needs the abutment platform before the surgical date.

Dentium suits a practice that wants one restorative connection across the bone-level systems the SuperLine page groups together, and that also wants a house graft line in Osteon and a collagen membrane. Surgical practices, restoring general dentists, and labs ordering abutments are all in that loop. The motor is separate. Read the implant motor guide for the console, and the bone-grafting guide before you treat Osteon as interchangeable with another company's particulate.

Immediate-loading language on the SuperLine and SuperLine II index lines is the manufacturer's indication statement. It is not a protocol you can copy onto Implantium or NR Line without their inserts. Narrow or short clinical situations need the specific length and diameter chart, which this profile does not reprint.

Offices outside the United States may be buying from a different Dentium distributor than Cypress. The about page's claim of more than 80 countries means the label and the warranty contact can differ. Ask which legal manufacturer is on the box you will open.

MIS is a Dentsply Sirona brand with a conical connection shared, in MIS's words, by C1 and V3. Implant Direct publishes Legacy as an internal hex and Simply Iconic as a conical hex, and it sells direct from Thousand Oaks. ZimVie publishes T3, TSX, and the older TSV and OSSEOTITE names from the Zimmer Biomet Dental lineage. Osstem and Straumann are other implant names in the product directory. None of these connections are a shared industry standard.

Dentium's own comparison point is internal. The SuperLine page says one connection and interchangeable abutments across three systems, which is an inventory argument if the chart confirms the systems you place. It is not an argument that a Dentium abutment fits an MIS or ZimVie implant.

On grafts, Osteon is Dentium's named synthetic or bone-graft family in the timeline. ZimVie publishes Puros allografts. MIS says it has regenerative products without the SKU list used here. Compare chemistry and handling in the grafting guide, then order the SKU your surgeon already knows how to use.

Pick the system from the current index, SuperLine, SuperLine II, Implantium, or NR Line, and order the surgical kit and prosthetic kit for that system even if abutments are shared. Confirm the three-system abutment claim against the latest compatibility chart before you throw away a second kit. Ask which fixtures are made at the Cypress address and which are made in Korea.

FDA clearance dates on the timeline are not a warranty. Ask Dentium USA for the implant warranty, the policy on unopened versus opened implants, and how long a drill is expected to last. The phone number printed with the Cypress address is 714-226-0229. Education through the study club is optional in the way the site describes it. It is still the fastest way to see the kit before you commit a full set of diameters.

Regenerative orders should name Osteon I or Osteon II and the membrane, not "Dentium graft." Particle size and the membrane's resorption claim are on the insert. If you also need a sinus kit, the timeline names an RS kit. Confirm it is still sold before you put it on a surgery calendar. The implant motor remains a separate capital item.