NobelReplace®

NobelReplace® Conical Connection PMC RP 5.0x11.5mm

Registry build 21.09.26
7manufacturers in China registered for this device type
121catalogue 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 NobelReplace®
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 2015-09-17
Record revised 2022-05-20 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Keep away from sunlight. Keep dry
Sizes Outer diameter 3.5 to 6 mm; length 8 to 16 mm
Distribution end date 2023-10-11

Catalogue Numbers

Catalogue numbers for NobelReplace®
Catalogue number Size Status
37295 Length 8.000 mm In distribution
36705 Outer Diameter 4.300 mm In distribution
37297 Outer Diameter 5.000 mm In distribution
37294 Length 16.000 mm In distribution
29434 In distribution
36710 Length 8.000 mm In distribution
37284 Length 8.000 mm In distribution
36702 Outer Diameter 3.500 mm In distribution
30087 Outer Diameter 6.000 mm In distribution
37299 Outer Diameter 5.000 mm In distribution
37288 Length 13.000 mm In distribution
37289 Outer Diameter 3.500 mm In distribution
36701 Length 11.500 mm In distribution
36709 Outer Diameter 4.300 mm In distribution
29435 In distribution
36714 Length 16.000 mm In distribution
37293 Length 13.000 mm In distribution
36713 Outer Diameter 5.000 mm In distribution
37291 Length 10.000 mm In distribution
36704 Outer Diameter 4.300 mm In distribution
36712 Outer Diameter 5.000 mm In distribution
36699 Length 8.000 mm In distribution
36700 Length 10.000 mm In distribution
37285 Outer Diameter 3.500 mm In distribution
37296 Outer Diameter 5.000 mm In distribution
37290 Length 8.000 mm In distribution
36703 Outer Diameter 3.500 mm In distribution
37287 Outer Diameter 3.500 mm In distribution
37292 Outer Diameter 4.300 mm In distribution
29433 In distribution
36711 Outer Diameter 5.000 mm In distribution
37298 Length 13.000 mm In distribution
36708 Outer Diameter 4.300 mm In distribution
29434 In distribution
30087 Outer Diameter 6.000 mm In distribution
36707 Length 11.500 mm In distribution
29433 In distribution
29435 In distribution
36902 Withdrawn
36103 Withdrawn
37294 Outer Diameter 4.300 mm Withdrawn
32218 Withdrawn
36699 Length 8.000 mm Withdrawn
32187 Withdrawn
36705 Outer Diameter 4.300 mm Withdrawn
36102 Withdrawn
36844 Withdrawn
32221 Withdrawn
36897 Withdrawn
32184 Withdrawn
32217 Withdrawn
36703 Length 16.000 mm Withdrawn
32213 Withdrawn
32216 Withdrawn
36899 Withdrawn
32906 Withdrawn
37298 Outer Diameter 5.000 mm Withdrawn
36714 Length 16.000 mm Withdrawn
32185 Withdrawn
36901 Withdrawn
32219 Withdrawn
37285 Outer Diameter 3.500 mm Withdrawn
37288 Outer Diameter 3.500 mm Withdrawn
37297 Length 11.500 mm Withdrawn
36900 Withdrawn
36895 Withdrawn
32910 Withdrawn
37296 Outer Diameter 5.000 mm Withdrawn
36898 Withdrawn
32160 Withdrawn
36842 Withdrawn
36843 Withdrawn
36712 Outer Diameter 5.000 mm Withdrawn
37299 Outer Diameter 5.000 mm Withdrawn
36710 Length 8.000 mm Withdrawn
32212 Withdrawn
32223 Withdrawn
36708 Length 13.000 mm Withdrawn
37293 Length 13.000 mm Withdrawn
32188 Withdrawn
36903 Withdrawn
32211 Withdrawn
32161 Withdrawn
36100 Withdrawn
37289 Length 16.000 mm Withdrawn
36702 Length 13.000 mm Withdrawn
36711 Outer Diameter 5.000 mm Withdrawn
36905 Withdrawn
32163 Withdrawn
37295 Length 8.000 mm Withdrawn
37287 Outer Diameter 3.500 mm Withdrawn
32908 Withdrawn
37284 Outer Diameter 3.500 mm Withdrawn
32220 Withdrawn
32181 Withdrawn
32214 Withdrawn
36896 Withdrawn
32182 Withdrawn
37291 Length 10.000 mm Withdrawn
36701 Outer Diameter 3.500 mm Withdrawn
36904 Withdrawn
32215 Withdrawn
32190 Withdrawn
36713 Outer Diameter 5.000 mm Withdrawn
32222 Withdrawn
36707 Outer Diameter 4.300 mm Withdrawn
36841 Withdrawn
32226 Withdrawn
37290 Outer Diameter 4.300 mm Withdrawn
32904 Withdrawn
36700 Outer Diameter 3.500 mm Withdrawn
37292 Length 11.500 mm Withdrawn
32225 Withdrawn
32162 Withdrawn
36704 Length 8.000 mm Withdrawn
32186 Withdrawn
36101 Withdrawn
32183 Withdrawn
32224 Withdrawn
32189 Withdrawn
36709 Outer Diameter 4.300 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 Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of NobelReplace®
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Nobel Biocare Services AG UDI-DI 2020-07-20 Class II Process control Dental implant cap label may incorrectly indicate implant measurements 5.0x8mm. Actual implant measurements are 4.3x10mm. If not noticed prior to implant placement, this could lead to: 1) A second surgical procedure; 2) Implant replacement; 188 2021-05-12

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