ZimVie Dental

Also known as: ZimVie, Zimmer Biomet Dental

The dental implant brand of ZimVie, carrying the T3, T3 PRO, TSX and Eztetic implant lines that descend from Zimmer Dental and Biomet 3i.

Key facts

Manufacturer	ZimVie Inc.Verified spec[1][2]
Parent company	ARCHIMED, which completed its acquisition of ZimVie on 20 October 2025Verified spec[3]
Country	United StatesVerified spec[3]
Headquarters	Palm Beach Gardens, Florida, United StatesVerified spec[3]
Ownership	Private since October 2025. ZimVie separated from Zimmer Biomet in 2021 as a listed company and was acquired by ARCHIMED in 2025, ending its Nasdaq listingVerified spec[3][1]
Predecessor system	Zimmer entered dentistry in 2003 by acquiring Centerpulse AG; Biomet acquired Implant Innovations (3i) in 1999; the two companies merged in 2011 to form Zimmer BiometVerified spec[1]
Prosthetic ecosystem	Implant lines named by the manufacturer include T3, T3 PRO, TSX, Eztetic and an immediate molar implant, supported by Encode impressions and GenTek restorative componentsManufacturer-reported[1][2]
manufacturingCountry	United States, Canada, SpainVerified spec[4]Country of the FDA-registered device establishment, which may differ from the brand’s home country.

Overview

This brand has been sold under several company names in twenty-five years, and patients often hold records under whichever one applied at the time — Implant Innovations, 3i, Biomet 3i, Zimmer Dental, Zimmer Biomet Dental and now ZimVie. The implants themselves persisted through those changes: the T3 line descends from the 3i side of the business and Tapered Screw-Vent from the Zimmer side. Ownership changed again in October 2025, when the investment firm ARCHIMED bought ZimVie and took it private. If you have an older implant from any of these names, the line name is the durable identifier; the company name on your paperwork will simply date it.

Regulatory record

Read this before drawing conclusions. A clearance or certificate means a device may legally be sold in a market. It is not a finding that the implant performs well, and it is not a comparison against other implants. In particular, FDA "clearance" is not FDA "approval" — clearance means the FDA accepted the device as substantially equivalent to one already on the market. What these actually mean →

Other5 records

Registered device establishment in United States. Registration records where a device is made or handled; it is not a clearance, an approval, or any assessment of the product.

Number	Device	Holder	Date
1038806	—	ZimVie US Corp LLC	—
1000244346	—	ZimVie Canada Inc.	—
3009840806	—	ZimVie Spain S.L.U.	—
3006411780	—	ZimVie Spain S.L.U.	—
1492 device records	—	ZimVie Dental	—

Clearance records for ZimVie Dental were retrieved from the issuing authority's own database, not from the manufacturer's marketing material. We attribute a clearance to a brand only when the filing holder belongs to that brand's corporate family — third-party clearances for compatible components are excluded, because they belong to the company that made the component, not to ZimVie Dental.

Sources

Numbers match the citations beside each claim above.

Primary sources

[1]We Are ZimVie — ZimVie Inc.. Accessed 2026-07-21.
[2]ZimVie Dental — homepage — ZimVie Inc.. Accessed 2026-07-21.
[3]ZimVie Announces Completion of its Acquisition by ARCHIMED — ZimVie Inc., 2025. Accessed 2026-07-21.
[4]openFDA — Device registrations and listings — US Food and Drug Administration. Accessed 2026-07-22.