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: KDC FDA class 1

Instrument, Surgical, Disposable

General, Plastic Surgery

View full classification →

A disposable surgical instrument is a single-use instrument intended for use during surgical procedures and then discarded, encompassing a wide variety of cutting, grasping, retracting, or dissecting tools across general and plastic surgery applications. It is classified as an FDA Class 1 device, the lowest risk tier, subject only to general controls and not requiring premarket notification. Product code KDC 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
DISPOSABLE SURGICAL SCISSORS AND FORCEPS
SURGIMED BREAST LOCALIZATION NEEDLE WIRE SET
THERMUFF BAG
MANUAL SURGICAL INSTRUMENTS
DISPOSABLE CAUTERY ABRASIVE PAD
INSTRUMENT ORGANIZER
SHUR-GRIP
DISPOSABLE INTRODUCER SHEATH
VESSELOOPS
BRADLEY TENACULUM HOLDER
RICHARD-ALLAN VESSEL LOOPS
KEY VASCULAR LOOPS
HOOK PROBE
BASKET FORCEP
PACIFIC GRASPER
SPOON
MAX-I-GRASP
ATLANTIC GRASPER
HOOK SCISSOR
INSTRUMENT MAKAR DISPOSALBE LOOP
SUTURE-AID BOOTIES
SDC VASCULAR TIES
PMT-OPTICA LINE
MICRO-EDGE DISPOSABLE BLADES
C-LOOPS
DRAVON T CLAMP
PLASTIC THUMB FORCEPS
DISPOSABLE FLOOR INSTRUMENTS
DISPOSABLE NEEDLE HOLDER
SAFETY PINS & RUBBER BANDS
DISPOSABLE SCISSORS
DISPOSABLE SCALPELS
DISPOSABLE HEMOSTAT (STRAIGHT&CURVED
DEVO'N LOOPS
NEGATIVE PRESSURE ARTERIAL BLOOD LINE
KAM SUCKER
KOLOR KODE TM
PEDIATRIC SUCKER
AXIOM LIG-A-BOOTS
OLSEN #770 DISPOSABLE HOLSTER
TIP-VU
TIP WIPE
CAUTERY CADDY PAD
SHARPS CADDY FB
ALTRACLUDE
FLEX-TEMPLATE
DAVIS & GECK NEEDLE/SHARPS COUNTER
SURGICAL STAPLE REMOVER
OMED SILICONE INSTRUMENT COVERS
SKIN STAPLE REMOVER

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.

Popular Product Codes

Commonly searched