Customed 712057831812
Customed 712057831812 (9001091812) is a Class II device made by Customed, Inc., cleared under FDA 510(k) K092338 on 27 May 2011 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI M20890010918120), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM20890010918120 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK092338 | Date27 May 2011 | StatusActive |
Official records
- FDA 510(k) database K092338
Across registries
- FDA 510(k) K092338 decided 27 May 2011 Active
- FDA GUDID UDI-DI M20890010918120 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K092338
- Listed FDA GUDID M20890010918120
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Customed
- Generic name
- Soft-tissue biopsy needle, single-use
- Model / Ref / Catalog
- 712057831812, 9001091812
- Primary DI / UDI-DI
- M20890010918120
- 510(k) Number
- FDA product code
- KNW
- GMDN term
- Soft-tissue biopsy needle, single-use
- Device class
- Class II
- Regulation number
- 876.1075
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 120 MillimeterNeedle Gauge — 18 Gauge
Similar devices
Other devices filed under FDA product code KNW (Instrument, Biopsy).
- MEDSOL GOLDENBERG BONE MARROW BIOPSY NEEDLE by Medsol Corp.
- CorVocet™ 00884450477489 CORA2020S/B by Merit Medical Systems, Inc.
- WANG/MILL-ROSE PLEURAL BIOPSY NEEDLE by Mill-Rose Laboratory
- AUTOMATED CORE BIOPSY DEVICE by Promex, Inc.
- Co-Axial Introducer Needle MCXS1808SX by Argon Medical Devices, Inc.
- DISPOSABLE BIOPSY FORCEP FOR FLEXIBLE ENDOSCOPES by Endo-Scientific, Inc.
- SuperCore™ Biopsy Instrument 701116200 by Argon Medical Devices, Inc.
- TEMNO Elite™ 00884450397848 TE1806 by Merit Medical Systems, Inc.
- MAMMOTOME EX HAND HELD SYSTEM by Ethicon Endo-Surgery, LLC
- Mammotome Revolve CA000507001 MSCM1 by Devicor Medical Products, Inc.