Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: LCJ FDA unclassified

Tissue Expander And Accessories

Unknown

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Tissue expanders and accessories are implantable medical devices used in plastic and reconstructive surgery to gradually stretch skin and soft tissue before final implant placement, such as in breast reconstruction following mastectomy. This device type is currently unclassified by the FDA, meaning formal classification has not been finalized and its regulatory pathway remains under review. The product code is LCJ, with no regulation number or medical specialty assigned. This device is flagged as an implant.

510(k) Clearances

50+ matches
K Number
Device Name
MENTOR™ PliaForm™ Breast Tissue Expander w/ Suture Tabs
Mentor™ CPX ™ 4 PLUS Enhance Breast Tissue Expander
MENTOR™ CPX™4 PLUS Enhance Breast Tissue Expander
Motiva Flora SmoothSilk Tissue Expander
AlloX2 Pro Tissue Expanders
Sientra, inc. Portfinder
Natrelle 133 Plus MICROCELL Tissue Expander
CPX 4 Breast Tissue Expander with Smooth Surface
Natrelle 133S Tissue Expander
Unger Quad Injector
ARTOURA Breast Tissue Expanders with Smooth Surface
CPX 4 Breast Tissue Expander
Natrelle 133 Plus Tissue Expander
Artoura Breast Tissue Expander
CPX Control Breast Tissue Expander
ALLOX2 TISSUE EXPANDERS
BLOSSOM SALINE DELIVERY ASSIST DEVICE
MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXPANDERS
LIFECELL TISSUE EXPANDER
NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS
SILICONE TISSUE EXPANDER
MENTOR CONTOUR PROFILE TISSUE EXPANDER
HUTCHISON INFLATABLE SILICONE TISSUE EXPANDERS
SEARE BIOMEDICAL SILICONE TISSUE EXPANDER
SILIMED TISSUE EXPANDER
MAGNETIC PORT SILICONE TISSUE EXPANDER
SILICONE TISSUE/INFLATABLE TISSUE EXPANDER
MENTOR INJECTION PORT DETECTOR (IPD)
ACCU-TEC SYSTEM FOR TISSUE EXPANDER INJECTION PORT
SURGITEK TEX-SPAN TEXTURED TISSUE EXPANDER
MENTOR TISSUE EXPANDERS W/TDMAC COATING
SURGITEK(R) EXTERNAL FILL PORT
SURGITEK FLAT T-SPAN
RADOVAN TISSUE EXPANDER (OPTION INTEGRAL INJECT.)
CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER
MCGHAN TISSUE EXPANDER FILL SYSTEM
POREX(TM) TISSUE EXPANDER
BREAST PROSTHESIS (NON & INFLATABLE) SKIN EXPANDER
MCGHAN LONGTERM MAMMARY EXPANDER, RTV DESIGN
MCGHAN LONGTERM MAMMARY EXPANDER/GEL-SALINE DESIGN
MCGHAN MAGNA-SITE(TM) TISSUE EXPANDER
MENTOR FLAT-SPAN
MCGHAN INTEGRAL VALVE TISSUE EXPANDER
MCGHAN TISSUE EXPANDER FILL KIT
TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600
MENTOR EXPANDER MAMMARY PROSTHESIS
CREAT BRAND SKIN EXPANDER
MCGHAN TISSUE EXPANDER
RADOVAN TISSUE EXPANDER
TISSUE EXPANDER

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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