Not currently registered with FDA under this name

Ace Surgical Supply Company, Inc.

Brockton, MA, United States. Named as applicant on 22 dental 510(k) clearances between 1994 and 2011. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
221994–2011
Markets registered in
39 registrations outside the US
Establishments
0—
1994: 41995: 21996: 31998: 11999: 12001: 12002: 12004: 12005: 12006: 12008: 22009: 12010: 22011: 11990200020102020

510(k) clearances per year, 1990–2026

Registered in 3 markets

Where regulators' registries name Ace Surgical Supply Company, Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 22 clearancesTaiwan: 8 registrationsPeru: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantAce Surgical Supply Company, Inc.22 clearances1994–2011Below
TaiwanTFDAManufacturerACE SURGICAL SUPPLY COMPANY, INC.82005–2016Pure Global AI
PeruDIGEMIDManufacturerACE SURGICAL SUPPLY CO., INC.12023–2023Pure 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 Ace Surgical Supply Company, Inc. as the applicant.

Decided510(k)DeviceDevice type
18 Aug 2011K103790ACE TRIMARK TRICAM DENTAL IMPLANTDZE Root-Form Endosseous Implant
20 Dec 2010K102981ACE FREEDOM INTERNAL HEXAGON DENTAL IMPLANT SYSTEMDZE Root-Form Endosseous Implant
14 Jan 2010K093518ACE SURGICAL SECURE LOCATOR 3.25 IMPLANT SYSTEMDZE Root-Form Endosseous Implant
16 Sep 2009K092594ACE SURGICAL SECURE- MINI LOCATOR IMPLANT SYSTEM, MODEL 09-2702-OX, 09-2703-OX, 09-2705-OXDZE Root-Form Endosseous Implant
13 Mar 2008K073343ACE SURGICAL SECURE-MINI IMPLANT SYSTEM, MODEL 09-270X-XXDZE Root-Form Endosseous Implant
14 Feb 2008K080074ACE SURIGICAL TRU-FIX IMPLANT SYSTEM, MODEL 454-180X-XXDZE Root-Form Endosseous Implant
16 Aug 2006K061397ACE SURGICAL ORTHODONTIC BONE SCREW SYSTEMS, 1.2/1.5 MM X 6MM,8MM, MODEL 454-91001,454-91002 AND 1.2/1.5MM X 6,8,10MM, MOAT Orthodontic Endosseous Implant
15 Jul 2005K051381ACE SURGICALPLASTER CALCIUM SULFACE HEMIHYDRATELYC Synthetic Bone Grafting Material
22 Jul 2004K041759ACE CONNECT INTERNAL CONNECTIONDZE Root-Form Endosseous Implant
3 May 2002K021244ACE HA SCREW DENTAL IMPLANT SYSTEMDZE Root-Form Endosseous Implant
2 Feb 2001K002075ACE SDS 3.75MM SCREW DENTAL IMPLANTDZE Root-Form Endosseous Implant
25 Mar 1999K990140NORMED BONE TRANSPORTJEY Bone Plate
6 Nov 1998K981526ACE ALVEOLAR DISTRACTORJEY Bone Plate
5 Jun 1996K954605ACE CYLINDER DENTAL IMPLANTDZE Root-Form Endosseous Implant
5 Jun 1996K954513ACE SREW DENTLA IMPLANT SYSTEMDZE Root-Form Endosseous Implant
6 Feb 1996K952847NORMED BIDIRECTRIONAL/MULTIDIRECTIONAL JAW DISTRACTORMQN External Mandibular Fixator and/or Distractor
25 Aug 1995K951510ACE BONE SCREW TACKING KITDZL Intraosseous Fixation Screw
5 May 1995K951392MINIBONEPLATE SYSTEMJEY Bone Plate
10 Jan 1994K922652ACE BASIC DENTAL IMPLANT PACK IEIA Operative Dental Unit
10 Jan 1994K922651ACE DENTAL IMPLANT KITEIA Operative Dental Unit
10 Jan 1994K922650ACE DENTAL IMPLANT CUSTOM SURGICAL PACKEIA Operative Dental Unit
10 Jan 1994K922649ACE BASIC DENTAL IMPLANT PACK IIEIA Operative Dental Unit

Some of these clearances are listed with FDA today by another company: BioHorizons Implant Systems, Inc. (3).

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.