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: KDD FDA class 1

Kit, Surgical Instrument, Disposable

General, Plastic Surgery

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A disposable surgical instrument kit is a pre-assembled, single-use collection of surgical tools packaged together for a specific procedure or general surgical use, intended to reduce processing time and eliminate the risk of cross-contamination associated with reusable instruments. It is classified as an FDA Class 1 device, the lowest risk category, subject only to general controls and not requiring premarket clearance. Product code KDD is regulated under 21 CFR 878.4800 in the General, Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURES
INSTRUMENTS FOR ONE TIME USE - DISPOSABLE
NATIONAL MEDICAL HEALTHCARE CUSTOM ORTHOPEDIC KITS AND TRAYS
DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAY
SUTURE SET OR LACERATION TRAYS (PACKS)
SURGICAL INSTRUMENT KIT, DISPOSABLE
KIT, SURGICAL INSTRUMENT, DISPOSABLE
BIOPSY/MYELO/ARTHRO/AMNIOCENT/BASIC SKIN PREP TRAY
STERILE SURGICAL INSTRUMENT TRAYS
DEXIDE LAPAROSCOPIC KITS
SURGICAL INSTRUMENT KIT, DISPOSABLE
LACERATTION TRAY
GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB
STERILE CUSTOM SURGICAL KITS
SLIP-PRUF-CLINGER
BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES
IN-SIGHT SURGICAL INSTRUMENT KITS, DISPOSABLE
MEGA GENERAL PURPOSE INSTRUMENT KIT
INCISION AND DRAINAGE KIT
DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)
SKILCRAFT
ENTERON ABDOMINAL PARACENTESIS TRAY
STERILE PROCEDURAL TRAYS
JMS HALO APPLICATION TRAY
SUTURE REMOVAL KIT
STERILE SUTURE REMOVAL KIT
C-SECTION TRAY
STERILE SOLUTION BOWL
STERILE SUTURE BOOTS
PREPACELL-STERILE-BONE MARROW ASPIR
VYGON THORACIC DRAINAGE-VARIOUS #'S
STERILE DISP. INSTRUMENT TRAYS
STERILE SUTURE REMOVAL SET
FIRST AID KITS
OPEN HEART TRAY (CUSTOM DESIGNED)
HEMO-NATE L-P KIT
STERILE SUTURE REMOVAL KIT
STERILE CATH CARE KIT
STERILE TRACHEOSTOMY CARE KIT
SUTURE REMOVAL TRAY
ACKRAD INCISION & DRAIN SET
SKIN SCRUB KITS
SUTURE REMOVAL SET(DISPLSABLE)
SUTURE REMOVAL KIT
EMERGENCY DEPARTMENT LACERATION KIT-
SUTURE REMOVAL SET CAT.#906
INSTRUMENT AND ACCESSORY KIT
STERILE SUTURE REMOVAL KIT
MAJOR SUTURE REMOVAL TRAY
SUTURE REMOVAL KIT

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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