NobelParallel™

NobelParallel™ Conical Connection NP 3.75x11.5mm

Registry build 21.09.26
7manufacturers in China registered for this device type
54catalogue 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 NobelParallel™
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 2023-10-12 (version 10)

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 3.75 to 5.5 mm; length 7 to 18 mm
Distribution end date 2023-10-11

Catalogue Numbers

Catalogue numbers for NobelParallel™
Catalogue number Size Status
37977 Length 7.000 mm In distribution
37979 Outer Diameter 5.000 mm In distribution
37986 Outer Diameter 5.500 mm In distribution
37982 Outer Diameter 5.000 mm In distribution
37981 Length 13.000 mm In distribution
37978 Outer Diameter 5.000 mm In distribution
37964 Outer Diameter 3.750 mm In distribution
37971 Outer Diameter 4.300 mm In distribution
37968 Outer Diameter 3.750 mm In distribution
37966 Outer Diameter 3.750 mm In distribution
37976 Length 18.000 mm In distribution
37973 Length 11.500 mm In distribution
37963 Length 7.000 mm In distribution
37985 Outer Diameter 5.500 mm In distribution
37967 Outer Diameter 3.750 mm In distribution
37987 Length 11.500 mm In distribution
37988 Outer Diameter 5.500 mm In distribution
37980 Length 11.500 mm In distribution
37975 Length 15.000 mm In distribution
37969 Length 18.000 mm In distribution
37983 Length 18.000 mm In distribution
37972 Length 10.000 mm In distribution
37984 Outer Diameter 5.500 mm In distribution
37989 Outer Diameter 5.500 mm In distribution
37970 Length 7.000 mm In distribution
37974 Length 13.000 mm In distribution
37965 Length 10.000 mm In distribution
37987 Outer Diameter 5.500 mm Withdrawn
37988 Length 13.000 mm Withdrawn
37973 Outer Diameter 4.300 mm Withdrawn
37979 Length 10.000 mm Withdrawn
37975 Length 15.000 mm Withdrawn
37976 Outer Diameter 4.300 mm Withdrawn
37970 Length 7.000 mm Withdrawn
37966 Length 11.500 mm Withdrawn
37982 Length 15.000 mm Withdrawn
37971 Outer Diameter 4.300 mm Withdrawn
37986 Length 10.000 mm Withdrawn
37974 Outer Diameter 4.300 mm Withdrawn
37968 Length 15.000 mm Withdrawn
37981 Outer Diameter 5.000 mm Withdrawn
37964 Length 8.500 mm Withdrawn
37969 Length 18.000 mm Withdrawn
37978 Length 8.500 mm Withdrawn
37985 Length 8.500 mm Withdrawn
37965 Length 10.000 mm Withdrawn
37989 Length 15.000 mm Withdrawn
37977 Length 7.000 mm Withdrawn
37963 Outer Diameter 3.750 mm Withdrawn
37983 Outer Diameter 5.000 mm Withdrawn
37967 Outer Diameter 3.750 mm Withdrawn
37980 Outer Diameter 5.000 mm Withdrawn
37984 Length 7.000 mm Withdrawn
37972 Length 10.000 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