Screw, Fixation, Bone

117 catalogue numbers from PP-0432, listed by Biomet Microfixation, United States, under Screw, Fixation, Bone. 31 manufacturers in China are registered for this product code.

Registry build 21.09.26
31manufacturers in China registered for this device type
117catalogue numbers in this listing
2510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (15), Shanghai (5), Zhejiang (3). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWC
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11

Showing 12 of 31. All 31 manufacturers in China registered for Screw, Fixation, Bone

Record

Regulatory record for Screw, Fixation, Bone
Listed by Biomet Microfixation, United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K063052
Record published 2018-03-15
Record revised 2025-06-09 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2020-07-27

Catalogue Numbers

Catalogue numbers for Screw, Fixation, Bone
Catalogue number Size Status
PP-0432 In distribution
PM619330 In distribution
323.0056 In distribution
PP-0419 In distribution
PP-0344 In distribution
PM619106 In distribution
PP-0414 In distribution
PP-0244 In distribution
PP-0436 In distribution
PP-0408 In distribution
323.0075 In distribution
PM619156 In distribution
PP-0449 In distribution
SP-2470 In distribution
323.1090 In distribution
PP-0362 In distribution
PP-0365 In distribution
PP-0267 In distribution
SP-2469 In distribution
PP-0340 In distribution
PP-0417 In distribution
PP-0406 In distribution
PP-0259 In distribution
PP-0331 In distribution
PP-0334 In distribution
PP-0351 In distribution
PM619208 In distribution
SP-1214 In distribution
SP-1665 In distribution
PP-0270 In distribution
PP-0343 In distribution
PP-0337 In distribution
PP-0356 In distribution
PP-0272 In distribution
SP-1464 In distribution
PP-0454 In distribution
PP-0320 In distribution
PM619324 In distribution
PP-0312 In distribution
PP-0397 In distribution
PP-0252 In distribution
323.1030 In distribution
323.0078 In distribution
PP-0329 In distribution
PP-0458 In distribution
323.1290 In distribution
PP-0357 In distribution
PM619320-A In distribution
323.1021 In distribution
PP-0364 In distribution
323.1011 In distribution
PP-0423 In distribution
PP-0376 In distribution
PP-0264 In distribution
323.0010 In distribution
PP-0385 In distribution
PP-0325 In distribution
323.1022 In distribution
PP-0445 In distribution
SP-3344 In distribution
PP-0342 In distribution
PP-0306 In distribution
PP-0420 In distribution
PP-0411 In distribution
PP-0258 In distribution
PP-0335 In distribution
PP-0395 In distribution
323.1202 In distribution
PP-0310 In distribution
323.1207 In distribution
PP-0327 In distribution
PP-0421 In distribution
PP-0440 In distribution
PP-0447 In distribution
323.1012 In distribution
PP-0373 In distribution
PM619283-A In distribution
323.1005 In distribution
323.1205 In distribution
PP-0453 In distribution
PP-0279 In distribution
PP-0313 In distribution
PP-0425 In distribution
SP-1465 In distribution
PP-0399 In distribution
PP-0277 In distribution
PP-0383 In distribution
323.1020 In distribution
PP-0261 In distribution
PP-0269 In distribution
SP-3340 In distribution
PP-0439 In distribution
PP-0262 In distribution
PP-0452 In distribution
PP-0384 In distribution
PP-0263 In distribution
323.1023 In distribution
PP-0416 In distribution
PP-0350 In distribution
915-2702 In distribution
PP-0456 In distribution
PP-0326 In distribution
PP-0392 In distribution
PP-0444 In distribution
PP-0274 In distribution
PP-0442 In distribution
SP-1424 In distribution
323.1010 In distribution
PP-0361 In distribution
323.1007 In distribution
323.1033 In distribution
PP-0341 In distribution
PP-0398 In distribution
PP-0368 In distribution
SP-2467 In distribution
SP-2470 Withdrawn
SP-2468 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Screw, Fixation, Bone Synthes Gmbh 3,975
Aptus Medartis Inc. 3,623
Acumed Acumed LLC 3,187
Arthrex® Arthrex, Inc. 2,781
OsteoMed Osteomed 2,764
Screw, Fixation, Bone AAP Implantate AG 2,176
Screw, Fixation, Bone Zimmer, Inc. 1,993
Arix System Bone Screw Jeil Medical Corporation 1,875
Cannulated Screw System + Tyber Medical 1,814
Cannulated Compression Headless Screw Tyber Medical 1,621
Microware Bone Plates and Bone Screws Microware Precision Co., Ltd. 1,601
Anthem Globus Medical, Inc. 1,538

Showing 12 of 5,775. All products under Screw, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K151173 2015-05-26
K111908 2011-11-29

Recalls

The FDA has not published a severity grade for these. 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
2010-05-17 Not classified Labeling mix-ups On May 17, 2010, Biomet Microfixation issued a Safety Alert on their Thinflap System Cross Drive, Self Drilling Screw, 1.5x4mm, Model #: 91-6704, Lot#: 173770. The product is labeled incorrectly. Some packages of 91-6704 lot 173770 are labe 927 2011-10-12
2009-09-15 Not classified Component change control Biomet Microfixation is recalling LactoSorb Self Drilling Adjustable Tap Model Numbers 915-2075 Lot # 064350 and 915-2185 Lot # 885580. The two lots identified have a new style stop and an old style tap; they are not compatible, as the dep 15 pieces 2010-01-23
2009-09-15 Not classified Component change control Biomet Microfixation is recalling LactoSorb Self Drilling Adjustable Tap Model Numbers 915-2075 Lot # 064350 and 915-2185 Lot # 885580. The two lots identified have a new style stop and an old style tap; they are not compatible, as the dep 7 pieces 2010-01-23

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