Rescue Internal Fixture

Rescue Internal Ø6.5/ L=11.5

Registry build 21.09.26
7manufacturers in China registered for this device type
35catalogue numbers in this listing
17510(k) clearances naming this product 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 Rescue Internal Fixture
Listed by Megagen Implant Co., Ltd., South Korea
FDA product code DZE
Device type Implant, Endosseous, Root-Form
Device class Class 2
Regulation 21 CFR 872.3640
Establishment Repacker / relabeller, Manufacturer, Exporter
Record published 2015-06-23
Record revised 2018-03-29 (version 2)

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, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Rescue Internal Fixture
Catalogue number Size Status
RSWIR7005 In distribution
RSWIR8013 In distribution
RSWIR6011 In distribution
RSWIR6013 In distribution
RSWIR7011 In distribution
RSWIR7513 In distribution
RSWIR6513 In distribution
RSWIR8006 In distribution
RSWIR6511 In distribution
RSWIR6008 In distribution
RSWIR6006 In distribution
RSWIR6508 In distribution
RSWIR7511 In distribution
RSWIR7007 In distribution
RSWIR6505 In distribution
RSWIR7510 In distribution
RSWIR7507 In distribution
RSWIR8011 In distribution
RSWIR6010 In distribution
RSWIR6007 In distribution
RSWIR6510 In distribution
RSWIR6005 In distribution
RSWIR8007 In distribution
RSWIR7505 In distribution
RSWIR7506 In distribution
RSWIR8008 In distribution
RSWIR6507 In distribution
RSWIR6506 In distribution
RSWIR7010 In distribution
RSWIR7008 In distribution
RSWIR8005 In distribution
RSWIR7013 In distribution
RSWIR7006 In distribution
RSWIR7508 In distribution
RSWIR8010 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
K251232 2026-06-18
K241972 2024-12-27
K231967 2023-12-07
K230618 2023-10-11
K223339 2023-07-18
K211812 2023-01-06
K203554 2021-08-28
K210161 2021-06-22
K192347 2019-11-14
K182448 2019-10-09
K191127 2019-10-08
K150537 2015-07-21
K140091 2014-12-12
K123988 2013-08-15
K123870 2013-03-27
K122231 2012-10-04
K081302 2008-08-15

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