Not currently registered with FDA under this name

Depuyacromed

Raynham, MA, United States. Named as applicant on 2 dental 510(k) clearances between 2001 and 2001. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
22001–2001
Markets registered in
467 registrations outside the US
Establishments
0—
2001: 2200020102020

510(k) clearances per year, 2000–2026

Registered in 4 markets

Where regulators' registries name Depuyacromed as the manufacturer or the registration holder of a device.

All markets
United States: 2 clearancesSouth Korea: 56 registrationsTaiwan: 10 registrationsCanada: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantDepuyacromed2 clearances2001–2001Below
South KoreaMFDSManufacturerDePuy AcroMed, Inc.DePuy AcroMed, Inc · DEPUY ACROMED INC. · +2561999–2003Pure Global AI
TaiwanTFDAManufacturerDEPUY ACROMED, INC.101989–1998Pure Global AI
CanadaHealth CanadaRegistration holderDEPUY ACROMED11999–1999Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Depuyacromed as the applicant.

Decided510(k)DeviceDevice type
1 Mar 2001K010320MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEMLYC Synthetic Bone Grafting Material
18 Jan 2001K003286SYMPHONY GRAFT DELIVERY SYSTEMLYC Synthetic Bone Grafting Material

Some of these clearances are listed with FDA today by another company: DePuy Spine, Inc. (2), Medos International SARL (1), DePuy Synthes, Inc. (1).

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.