Natural-Knee®

143 catalogue numbers from 6225-19-095, listed by Zimmer, Inc., United States, under Template. 21 manufacturers in China are registered for this product code.

Registry build 21.09.26
21manufacturers in China registered for this device type
143catalogue numbers in this listing
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (3), Zhejiang (2). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWT
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Guangzhou Clean Medical Products Manufacturing Corp Guangzhou Guangdong Contract manufacturer 5
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Showing 12 of 21. All 21 manufacturers in China registered for Template

Record

Regulatory record for Natural-Knee®
Listed by Zimmer, Inc., United States
FDA product code HWT
Device type Template
Device class Class 1
Regulation 21 CFR 888.4800
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-12-28
Record revised 2022-03-22 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Sizes Length 90 to 215 mm

Catalogue Numbers

Catalogue numbers for Natural-Knee®
Catalogue number Size Status
6225-19-095 9.5 mm X 190 mm In distribution
6279-08-112 Size 2, 8 mm In distribution
6308-09-311 Size 3, 9mm In distribution
6299-00-250 In distribution
6308-22-211 Size 2, 22mm In distribution
6308-19-411 Size 4, 19mm In distribution
6291-00-340 Size 4 In distribution
6308-11-112 Size 00, 11mm In distribution
6279-01-203 Size 00 In distribution
6279-04-112 Size 2, 4 mm In distribution
6191-03-013 13.0 mm In distribution
6308-22-112 Size 00, 22mm In distribution
6308-11-311 Size 3, 11mm In distribution
6291-00-300 Length 120 mm In distribution
6308-09-112 Size 00, 9mm In distribution
6279-01-200 Size 0 In distribution
6308-04-100 Size 00-0 In distribution
6275-75-105 10.5 mm X 75 mm In distribution
6308-22-411 Size 4, 22mm In distribution
6308-16-411 Size 4, 16mm In distribution
6291-16-006 Length 200 mm In distribution
6291-16-005 Length 125 mm In distribution
6279-01-240 Size 4 In distribution
6308-16-511 Size 5, 16mm In distribution
6308-25-511 Size 5, 25mm In distribution
6279-04-015 Size 5, 4 mm In distribution
6308-09-111 Size 1, 9mm In distribution
6279-00-131 8 mm In distribution
6291-00-302 Length 155 mm In distribution
6308-11-111 Size 1, 11mm In distribution
6279-04-110 Size 0, 4 mm In distribution
6308-19-511 Size 5, 19mm In distribution
6225-19-185 18.5 mm X 190 mm In distribution
6308-09-511 Size 5, 9mm In distribution
6290-00-709 4-Prong In distribution
6279-00-200 Size 0 In distribution
6279-08-111 Size 1, 8 mm In distribution
6279-08-010 Size 0, 8 mm In distribution
6291-01-002 Size 2 In distribution
6308-09-211 Size 2, 9mm In distribution
6279-08-014 Size 4, 8 mm In distribution
6225-19-105 10.5 mm X 190 mm In distribution
6191-03-009 9.0 mm In distribution
6279-01-210 Size 1 In distribution
6308-13-011 Size 0, 13mm In distribution
6279-08-114 Size 4, 8 mm In distribution
6308-19-112 Size 00, 19mm In distribution
6308-16-211 Size 2, 16mm In distribution
6279-04-011 Size 1, 4 mm In distribution
6191-01-013 13.0 mm In distribution
6291-00-303 6.0 Degrees In distribution
6279-08-011 Size 1, 8 mm In distribution
6225-19-115 11.5 mm X 190 mm In distribution
6308-11-211 Size 2, 11mm In distribution
6308-25-112 Size 00, 25mm In distribution
6191-02-013 13.0 mm In distribution
6308-25-111 Size 1, 25mm In distribution
6291-00-298 Length 90 mm In distribution
6279-08-000 Size 00, 8 mm In distribution
6279-04-013 Size 3, 4 mm In distribution
6279-04-111 Size 1, 4 mm In distribution
6291-16-004 10.5 mm Diameter In distribution
6308-19-211 Size 2, 19mm In distribution
6279-04-012 Size 2, 4 mm In distribution
6225-19-195 19.5 mm X 190 mm In distribution
6308-13-111 Size 1, 13mm In distribution
6308-13-112 Size 00, 13mm In distribution
6279-00-130 4 mm In distribution
6291-00-370 Size 1/2 +14 mm In distribution
6308-04-300 Size 3-5 In distribution
6279-01-230 Size 3 In distribution
6279-01-220 Size 2 In distribution
6308-16-111 Size 1, 16mm In distribution
6291-16-003 Length 125 mm In distribution
6291-00-304 5.0 Degrees In distribution
6290-00-542 In distribution
6279-04-010 Size 0, 4 mm In distribution
6191-01-011 11.0 mm In distribution
6279-00-203 Size 00 In distribution
6291-00-310 Size 1 In distribution
6191-01-009 9.0 mm In distribution
6291-00-320 Size 2 In distribution
6308-13-411 Size 4, 13 mm In distribution
6279-04-014 Size 4, 4 mm In distribution
6279-08-013 Size 3, 8 mm In distribution
6279-08-113 Size 3, 8 mm In distribution
6308-09-011 Size 0, 9mm In distribution
6225-19-155 15.5 mm X 190 mm In distribution
6308-19-311 Size 3, 19mm In distribution
6279-08-115 Size 5, 8 mm In distribution
6308-16-311 Size 3, 16mm In distribution
6308-13-311 Size 3, 13mm In distribution
6308-25-311 Size 3, 25mm In distribution
6308-16-112 Size 00, 16mm In distribution
6225-19-125 12.5 mm X 190 mm In distribution
6291-01-001 Size 1 In distribution
6308-09-411 Size 4, 9mm In distribution
6308-19-011 Size 0, 19mm In distribution
6225-19-135 13.5 mm X 190 mm In distribution
6279-00-230 Size 3 In distribution
6291-16-002 Length 200 mm In distribution
6279-04-115 Size 5, 4 mm In distribution
6279-04-000 Size 00, 4 mm In distribution
6291-00-380 Size 2/3 +14 mm In distribution
6308-22-011 Size 0, 22mm In distribution
6291-01-000 Size 0 In distribution
6225-19-165 16.5 mm X 190 mm In distribution
6191-02-009 9.0 mm In distribution
6308-25-411 Size 4, 25mm In distribution
6308-25-211 Size 2, 25mm In distribution
6279-00-112 In distribution
6291-01-003 Size 3 In distribution
6308-11-411 Size 4, 11mm In distribution
6279-08-012 Size 2, 8 mm In distribution
6308-22-511 Size 5, 22mm In distribution
6308-11-511 Size 5, 11mm In distribution
6308-11-011 Size 0, 11mm In distribution
6279-00-250 Size 5 In distribution
6279-08-110 Size 0, 8 mm In distribution
6291-00-390 Size 3/4 +14 mm In distribution
6279-04-113 Size 3, 4 mm In distribution
6279-01-250 Size 5 In distribution
6279-04-114 Size 4, 4 mm In distribution
6308-22-111 Size 1, 22mm In distribution
6191-02-011 11.0 mm In distribution
6308-19-111 Size 1, 19mm In distribution
6308-16-011 Size 0, 16mm In distribution
6279-00-240 Size 4 In distribution
6291-00-360 Size 0/1 +14 mm In distribution
6279-00-210 Size 1 In distribution
6308-25-011 Size 0, 25mm In distribution
6279-08-100 Size 00, 8 mm In distribution
6225-19-145 14.5 mm X 190 mm In distribution
6308-13-211 Size 2, 13mm In distribution
6308-13-511 Size 5, 13mm In distribution
6279-00-220 Size 2 In distribution
6279-04-100 Size 00, 4 mm In distribution
6279-08-015 Size 5, 8 mm In distribution
6291-00-330 Size 3 In distribution
6308-04-200 Size 1-2 In distribution
6191-03-011 11.0 mm In distribution
6291-16-001 Length 125 mm In distribution
6308-22-311 Size 3, 22mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Attune Depuy (Ireland) 1,385
Template Exactech, Inc. 1,277
4WEB Medical 4WEB Inc. 991
Evolution® Microport Orthopedics Inc. 966
Template Zimmer, Inc. 792
Advance® Microport Orthopedics Inc. 644
Apex Knee System Omni Life Science, Inc. 635
Profemur® Microport Orthopedics Inc. 591
Link Instruments – Trial implants and size gauges Waldemar Link GmbH & Co. KG 549
Template Synthes Gmbh 516
Optetrak Logic Exactech, Inc. 512
Template Depuy Spine, Inc. 451

Showing 12 of 2,940. All products under Template

Recalls

27 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 Closed
2013-11-19 Class II Labeling design This is an expansion of the June 2013 recall of NexGen Micro components. Five (5) additional instruments have been identified that are associated only with the NexGen Micro components. There is the potential for these devices to be inadve 439 units 2015-05-06
2013-11-19 Class II Labeling design This is an expansion of the June 2013 recall of NexGen Micro components. Five (5) additional instruments have been identified that are associated only with the NexGen Micro components. There is the potential for these devices to be inadve 638 units 2015-05-06
2013-11-19 Class II Labeling design This is an expansion of the June 2013 recall of NexGen Micro components. Five (5) additional instruments have been identified that are associated only with the NexGen Micro components. There is the potential for these devices to be inadve 684 units 2015-05-06
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 all lots, all sizes 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 all lots, all sizes 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231, 641 all lots 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 all lots, all sizes 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 all lots, all sizes 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231641 all sizes 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231, 641 all lots 2014-05-16
2011-04-01 Class II Device Design Complaints have been received reporting sub-optimal fit between provisional femoral heads (VerSys and MIS) and the mating components (ie stems and provisional femoral necks), in some cases alleging the fit was too loose and in other cases, 231,641 all lots, all sizes 2014-05-16
2010-11-15 Not classified Employee error Mislabeled – Device packages labeled as hooded trial inserts contain standard trial inserts. 3 2011-05-23
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 56,516 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 128,946 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 128,946 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 56,516 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 56,516 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 128,946 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 56,516 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 56,516 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 56,516 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 128,946 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 128,946 all lots, all sizes 2014-04-30
2010-10-10 Class II Device Design Surgical technique instructions for the Versys and Slotted Provisional Femoral Heads have been enhanced to inform users that the head may become difficult to visually locate if it becomes displaced deep or medial to the iliopsoas tendon and 128,946 all lots, all sizes 2014-04-30
2008-12-12 Not classified Employee error Some 12 mm thick devices may have been etched and packaged as 14 mm thick, and vice versa. 131 of both products. 2009-11-12
2008-12-12 Not classified Employee error Some 12 mm thick devices may have been etched and packaged as 14 mm thick, and vice versa. 131 of both products. 2009-11-12
2006-10-19 Not classified Other The instrument may fracture at the threaded end during intramedullary trialing and leave the distal pilot trial in the humeral canal. 50 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05
2006-06-16 Not classified Other During provisional trialing, the instrument may become stuck in the humeral canal and require surgical removal. 324 total 2007-12-05

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