Peca® 2.0

Beveled compressive implant Ø4 lg42

Registry build 21.09.26
31manufacturers in China registered for this device type
54catalogue numbers in this listing
3510(k) clearances naming this product 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 Peca® 2.0
Listed by Novastep, France
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Manufacturer
Record published 2025-06-17
Record revised 2025-12-15 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Peca® 2.0
Catalogue number Size Status
PS060048 In distribution
PS060058 In distribution
PS070016 In distribution
PS060054 In distribution
PS060142 In distribution
PS070034 In distribution
PS060136 In distribution
PS060138 In distribution
PS060038 In distribution
PS060126 In distribution
PS060050 In distribution
PS060046 In distribution
PS060144 In distribution
PS060146 In distribution
PS060160 In distribution
PS070040 In distribution
PS070038 In distribution
PS070032 In distribution
PS060032 In distribution
PS070020 In distribution
PS070024 In distribution
PS070042 In distribution
PS060122 In distribution
PS060130 In distribution
PS070036 In distribution
PS060036 In distribution
PS060026 In distribution
PS060040 In distribution
PS060150 In distribution
PS070022 In distribution
PS060028 In distribution
PS060124 In distribution
PS070044 In distribution
PS060118 In distribution
PS070026 In distribution
PS060155 In distribution
PS060030 In distribution
PS060120 In distribution
PS070030 In distribution
PS070018 In distribution
PS060128 In distribution
PS060148 In distribution
PS070048 In distribution
PS070028 In distribution
PS060042 In distribution
PS060056 In distribution
PS070046 In distribution
PS060044 In distribution
PS060134 In distribution
PS060132 In distribution
PS060140 In distribution
PS060060 In distribution
PS060052 In distribution
PS060034 In distribution

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
K223468 2023-08-30
K143146 2015-02-06
K143229 2015-02-06

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