NobelActive®

NobelActive® Internal NP 3.5x11.5mm

Registry build 21.09.26
7manufacturers in China registered for this device type
56catalogue numbers in this listing
31510(k) clearances naming this product code
2recalls on this code

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 NobelActive®
Listed by Nobel Biocare AB, Sweden
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Specification developer, Manufacturer
Record published 2019-07-09
Record revised 2023-10-12 (version 8)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Keep away from sunlight. Keep dry
Sizes Length 7 to 18 mm; outer diameter 3 to 5.5 mm
Distribution end date 2023-10-11

Catalogue Numbers

Catalogue numbers for NobelActive®
Catalogue number Size Status
37806 Length 7.000 mm In distribution
36769 Outer Diameter 3.000 mm In distribution
34127 Outer Diameter 3.500 mm In distribution
35215 Length 18.000 mm In distribution
36772 Length 15.000 mm In distribution
35225 Outer Diameter 5.000 mm In distribution
37807 Outer Diameter 5.500 mm In distribution
37810 Length 13.000 mm In distribution
34137 Outer Diameter 5.000 mm In distribution
36771 Length 13.000 mm In distribution
36770 Outer Diameter 3.000 mm In distribution
37808 Outer Diameter 5.500 mm In distribution
37811 Outer Diameter 5.500 mm In distribution
34140 Outer Diameter 5.000 mm In distribution
34131 Outer Diameter 4.300 mm In distribution
34125 Length 10.000 mm In distribution
35223 Length 8.500 mm In distribution
34138 Outer Diameter 5.000 mm In distribution
35221 Length 8.500 mm In distribution
34126 Outer Diameter 3.500 mm In distribution
34133 Outer Diameter 4.300 mm In distribution
37809 Length 11.500 mm In distribution
35220 Length 18.000 mm In distribution
34134 Length 15.000 mm In distribution
35219 Length 18.000 mm In distribution
34128 Length 15.000 mm In distribution
34132 Length 11.500 mm In distribution
34139 Outer Diameter 5.000 mm In distribution
34127 Outer Diameter 3.500 mm Withdrawn
35221 Outer Diameter 3.500 mm Withdrawn
34128 Length 15.000 mm Withdrawn
37806 Length 7.000 mm Withdrawn
34133 Length 13.000 mm Withdrawn
36769 Outer Diameter 3.000 mm Withdrawn
34126 Outer Diameter 3.500 mm Withdrawn
37807 Length 8.500 mm Withdrawn
35225 Length 8.500 mm Withdrawn
34140 Outer Diameter 5.000 mm Withdrawn
36771 Outer Diameter 3.000 mm Withdrawn
34139 Outer Diameter 5.000 mm Withdrawn
34137 Length 10.000 mm Withdrawn
37808 Outer Diameter 5.500 mm Withdrawn
34125 Outer Diameter 3.500 mm Withdrawn
34134 Outer Diameter 4.300 mm Withdrawn
34131 Length 10.000 mm Withdrawn
34132 Outer Diameter 4.300 mm Withdrawn
37809 Outer Diameter 5.500 mm Withdrawn
37810 Outer Diameter 5.500 mm Withdrawn
34138 Outer Diameter 5.000 mm Withdrawn
37811 Outer Diameter 5.500 mm Withdrawn
35223 Outer Diameter 4.300 mm Withdrawn
36770 Outer Diameter 3.000 mm Withdrawn
35215 Length 18.000 mm Withdrawn
35220 Outer Diameter 5.000 mm Withdrawn
35219 Length 18.000 mm Withdrawn
36772 Outer Diameter 3.000 mm Withdrawn

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
K252197 2026-02-18
K243834 2025-08-25
K212125 2021-09-24
K202344 2020-11-16
K173418 2019-02-21
K183069 2018-12-04
K172352 2017-10-20
K170135 2017-05-11
K161598 2017-03-14
K160119 2016-06-02
K152836 2016-04-11
K152093 2016-03-16
K142260 2015-05-11
K133731 2014-05-08
K102436 2010-12-09
K083205 2009-02-13
K081128 2008-11-07
K070857 2007-12-28
K072980 2007-12-20
K071370 2007-08-03
K070182 2007-04-04
K061971 2007-03-06
K063718 2007-01-05
K062936 2006-12-19
K061003 2006-06-30
K050406 2005-06-08
K050705 2005-05-19
K050393 2005-05-04
K050258 2005-04-19
K030685 2004-02-06
K022562 2002-10-11

Recalls

2 of these are 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
2025-01-10 Class II Process control Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the finished product. 1,558 units (90 units – U.S.)
2022-07-25 Class II Process change control Due to the presence of a burr which may cause an aspiration risk to patient during surgical procedure. 347 devices

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