TRI-CAM Dental Implant System

TRI-CAM Multi-Unit Abutment STR 4MM H FOR 4.3MM 30 DEG Angle

Registry build 21.09.26
7manufacturers in China registered for this device type
33catalogue numbers in this listing
11510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (3), Sichuan (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DZE
Manufacturer City Province Registered as Device types
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Jiangsu Trausim Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 3
Basic (Chengdu) Medical Device Co., Ltd. Chengdu Sichuan Contract manufacturer 1
Dongguan Xinlonghong Hardware Co., Ltd. Dongguan Guangdong Contract manufacturer 1
Chengdu Besmile Medical Technology Co., Ltd. Chengdu Sichuan Manufacturer 14
BIO Concept Co., Ltd. Changzhou Jiangsu Manufacturer 5

Record

Regulatory record for TRI-CAM Dental Implant System
Listed by Ace Surgical Supply Co., Inc., United States
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
510(k) K103790
Record published 2015-10-24
Record revised 2019-11-08 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Length 3.5 to 13 mm; width 4.3 to 5 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for TRI-CAM Dental Implant System
Catalogue number Size Per pack Status
315011 Length 11 mm In distribution
30500001 Length 5 mm In distribution
314311 Length 11 mm In distribution
30843GL In distribution
305060 Length 6 mm In distribution
3011439 Length 4.3 mm In distribution
315016 Length 13 mm In distribution
30835GL In distribution
3043MU30 In distribution
3011509 Length 5 mm In distribution
3010351 Length 3.5 mm In distribution
3010352 Length 3.5 mm In distribution
30351702 Length 3.5 mm In distribution
315013 Length 13 mm In distribution
30350001 Length 3.5 mm In distribution
314313 Length 13 mm In distribution
3011359 Length 3.5 mm In distribution
3010431 Length 4.3 mm In distribution
3010501 Length 5 mm In distribution
3011508 Length 5 mm In distribution
314310 Length 10 mm In distribution
3011358 Length 3.5 mm In distribution
3011438 Length 4.3 mm In distribution
303560 Length 6 mm In distribution
3035MUA In distribution
3043MU17 Length 4.3 mm In distribution
3035S Length 3.5 mm 5 In distribution
30850GL In distribution
315010 Length 10 mm In distribution
315008 Length 8 mm In distribution
30431702 Length 4.3 mm In distribution
314308 Length 8 mm In distribution
314316 Length 13 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neodent Jjgc Indústria e Comércio de Materiais Dentários S.A. 920
Osstem Implant System Osstem Implant Co., Ltd. 788
Magicore InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) 744
Implant, Endosseous, Root-Form Southern Implants (PTY) Ltd 608
ITL Dental Emery Enterprises Inc. 603
Magicore S InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) 560
Friadent® Dentsply Implants Manufacturing GmbH 525
Sphero Block Normo Rhein 83 SRL 489
Neobiotech Implant System Neobiotech Co., Ltd. 483
KJ Mini Implant System Kjmeditech.co., Ltd. 448
Ritter Dental Implant System Ritter Implants GmbH & Co. KG 418
Leone SPA Leone SPA 404

Showing 12 of 2,762. All products under Implant, Endosseous, Root-Form

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K103790 2011-08-18
K102981 2010-12-20
K093518 2010-01-14
K092594 2009-09-16
K073343 2008-03-13
K080074 2008-02-14
K041759 2004-07-22
K021244 2002-05-03
K002075 2001-02-02
K954605 1996-06-05
K954513 1996-06-05

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2017-02-22 Class II Labeling mix-ups Incorrect device was packaged. 87 2017-08-07

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P800035 2001-10-04 PERI-OSS Curasan AG
P860012 1988-10-28 ALVEOFORM TM BIOGRAFT Collagen Corp.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer