OsteoJ

DISPOSABLE BONE MARROW BIOPSY NEEDLE WITH EXTRACTION WIRE AND SAFETY 11G x 100 mm

Registry build 21.09.26
2manufacturers in China registered for this device type
10catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Jiangsu (1), Zhejiang (1).

Chinese manufacturers registered for FDA product code DWO
Manufacturer City Province Registered as Device types
Hospital & Homecare IMP. & EXP. Co., Ltd. Nanjing Jiangsu Contract manufacturer 179
Wenzhou Aochang Misawa Medical Tech. Co., Ltd. Wenzhou Zhejiang Manufacturer 4

Record

Regulatory record for OsteoJ
Listed by M.D.L. S.R.L., Italy
FDA product code DWO
Device type Needle, Biopsy, Cardiovascular
Device class Class 1
Regulation 21 CFR 878.4800
Establishment Contract manufacturer, Manufacturer
Premarket notification Exempt
Record published 2021-05-14
Record revised 2021-05-27 (version 4)

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Pack of 10
Sizes Length 60 to 150 mm; needle gauge 8 to 13 G
Distribution end date 2021-05-14

Catalogue Numbers

Catalogue numbers for OsteoJ
Catalogue number Size Status
PJ0810 Length 100 mm In distribution
PJ1306 Length 60 mm In distribution
PJ1110 Length 100 mm In distribution
PJ1115 Length 150 mm In distribution
PJ0815 Length 150 mm In distribution
PJ1306 Withdrawn
PJ0810 Withdrawn
PJ0815 Withdrawn
PJ1110 Withdrawn
PJ1115 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
M-Biopsy Needle For Reusable Biopsy Instruments Mermaid Medical A/S 55
Biocore II MG Histo S.A. 33
Biocore II TC Histo S.A. 26
UltraCore™ Biopsy Needle Argon Medical Devices, Inc. 18
Illy M.D.L. S.R.L. 16
Biocore II BR Histo S.A. 15
PenBone M.D.L. S.R.L. 14
Biocore II Histo S.A. 14
PickUp M.D.L. S.R.L. 12
Custom Healthcare Systems, Inc. Manus Medical, LLC 11
PressTo M.D.L. S.R.L. 10
Mamawire Plus Histo S.A. 6

Showing 12 of 28. All products under Needle, Biopsy, Cardiovascular

Recalls

1 of these is 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
2021-08-05 Class II Other Sterility assurance may be compromised. 21,518 units 2026-05-04

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