Manufacturer registered with FDA

IDOC Dental Lab

Orange, CA, United States. Lists 11 dental device types with FDA across 1 registered establishment.

FDA owner/operator10059837Contract manufacturerRepacker / relabeler
Device types listed
11
Brands and models
36
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What IDOC Dental Lab currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Porcelain PowderEIH · Class 2Dental ceramics & zirconiaMaker
ADD-Z; Alpha+; MaxZir; Natura M; Natura S; NaturaZ HT; NaturaZ Illusion; NaturaZ Series (B16, B20, B42, B60, B98, B100)Chairside Zirconia; Perfit FS Dental Zirconia Fully Sintered Block; RAYZir FSChairside Zirconia; Perfit FS; RAYZir FSPerfit CLPerfit ZR HT Dental Zirconia blankPerfit ZR ST Dental Zirconia blank, Perfit ZR UT Dental Zirconia blank
2024
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsLister
Abutment, implant, dental, endosseousDenQ Sub Multi-unit Abutment(Angled-1) DSMAR493017OSDenQ Sub Multi-unit Abutment(Angled-1) DSMAR494017OSDenQ Sub Multi-unit Abutment(Angled-1) DSMAR494030OSDenQ Sub Multi-unit Abutment(Straight) DSMR48302SDenQ Sub Multi-unit Abutment(Straight) DSMR48402SDenQ Sub Multi-unit Abutment(Straight) DSMR48502SDenQ Sub Multi-unit Healing Cap MHC48DenQ Sub Multi-unit Lab Analog DMLA480DenQ Sub Multi-unit Pick-up Impression Coping MPIC480S
2 more
DenQ Sub Multi-unit Temporary Cylinder MTC480SSIMDA Abutment; SIMDA Lab Analog; SIMDA Scan Body
2024
Root-Form Endosseous ImplantDZE · Class 2Dental implantsLister
DenQ Sub Multi-unit Abutment(Angled-1) DSMAR493017OSDenQ Sub Multi-unit Abutment(Angled-1) DSMAR494017OSDenQ Sub Multi-unit Abutment(Angled-1) DSMAR494030OSDenQ Sub Multi-unit Abutment(Straight) DSMR48302SDenQ Sub Multi-unit Abutment(Straight) DSMR48402SDenQ Sub Multi-unit Abutment(Straight) DSMR48502SDenQ Sub Multi-unit Healing Cap MHC48DenQ Sub Multi-unit Lab Analog DMLA480DenQ Sub Multi-unit Pick-up Impression Coping MPIC480SDenQ Sub Multi-unit Temporary Cylinder MTC480S
2026
Resin Tooth Shade MaterialEBF · Class 2Dental compositesMaker
Rodin 3D Ceramic Nanohybrid Resin; Rodin Sculpture 2; Rodin Titan
2024
Resin Impression Tray MaterialEBH · Class 1Impression traysLister
JB Fork, JB Tray
2024
Rebasing Repairing Relining Denture ResinEBI · Class 2Denture resins & teethMaker
Lucitone Digital Print
2024
Cartridge SyringeEJI · Class 2Dental needles & syringesLister
I-JECT; i-JECT BuilT in System
2024
FacebowKCR · Class 1Articulators & facebowsLister
ADD POP BOW
2024
Anti-Snoring DeviceLRK · Class 2Anti-snoring & jaw-repositioning devicesMaker
EMA
2024
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
DentaGUIDE, DentaTRY
2024
Animal Source Bone Grafting MaterialNPM · Class 2Bone grafts & membranesLister
BONE GRAFTING MATERIAL, ANIMAL SOURCE
2024

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Also lists devices cleared under other names

IDOC Dental Lab lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: DenQ Co., Ltd. (1), MEDPARK.Co., Ltd. (1), Simda Co., Ltd. (1), KJ Meditech Co., Ltd. (1).

Decided510(k)DeviceApplicantDevice type
13 Sep 2024K240977DenQ Sub SLA Implant SystemDenQ Co., Ltd.DZE Root-Form Endosseous Implant
13 Oct 2023K231672S1MEDPARK.Co., Ltd.NPM Animal Source Bone Grafting Material
24 May 2023K223663SIMDA AbutmentSimda Co., Ltd.NHA Endosseous Dental Implant Abutment
8 Aug 2012K112787KERATORKJ Meditech Co., Ltd.NHA Endosseous Dental Implant Abutment

Registered establishments

EstablishmentLocationWhat it does
IDOC DENTAL LABFDA reg. 3013934196Orange, CA, United StatesContract manufacturer, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10059837). 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.