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: ETD FDA class 2

Tube, Tympanostomy

Ear, Nose, Throat

View full classification →

The tympanostomy tube (also known as a pressure equalization tube) is a small implantable device surgically inserted through the tympanic membrane to ventilate the middle ear, relieve fluid accumulation, and reduce recurrent ear infections in patients with chronic otitis media with effusion. It is classified as FDA Class 2, requiring 510(k) premarket clearance. The product code is ETD, regulated under 21 CFR 874.3880 in the Ear, Nose, Throat specialty. This device is designated as an implant.

510(k) Clearances

50+ matches
K Number
Device Name
Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy Tube Handpiece (Catalogue #: 12115-100-000) and Solo+ Tympanostomy Tube Cartridge (Catalogue #: 12115-200-000))
Solo+ Tympanostomy Tube Device (TTD)
Biowy Tym Tube (TT)
Tympanostomy Tubes
Hummingbird Tympanostomy Tube System
Hummingbird Tympanostomy Tube System
TULA Tube Delivery System
Hummingbird Tympanostomy Tube
Ventilation (Tympanostomy) Tubes
HUMMINGBIRD(TM) TYMPANOSTOMY TUBE SYSTEM (TTS)
PRECEPTIS TYMPANOSTOMY TUBE INSERTER
ACCLARENT TYMPANOSTOMY TUBE AND TYMPANOSTOMY TUBE DELIVERY SYSTEM
TYMPANOSTOMY TUBE
TROCAR VENTILATION TUBE/WITH TROCAR TIP, TROCAR HANDLE, MODEL 1015 074, 1015 076, 1015 075, 1015 077, W/ RETENTION WIRE
OTOMEDICS SOFT TYMPANOSTOMY TUBE
GRACE MEDICAL PC COATED TYMPANOSTOMY TUBES
BLUE PTFE (FLUOROPLASTIC) VENTILATION TUBES
NEOZOLINE VENTILATION TUBES
MICRODOSE CATH, MODELS 90121-201, -202, -203
PC COATED FLUOROPLASTIC VENT TUBES
FLUOROPLASTIC VENTILATION TUBES
SILVERSTEIN MICROWICK
EXMOOR MYRINGOTOMY KIT
TYMPANOSTOMY TUBE
PFLEIDERER'S INTRATYMPANIC CATHETER
ROUND WINDOW E-CATH
SHAH PERMAVENT
TUBINGEN TYMPANIC VENTILATION TUBE, TYMPANIC VENTILATION TUBES WITH ENE/S, DIABOLO TYMPANIC VENTILATION TUBE, MINIMAL T)
MYRINGOTOMY TUBE
MYRINGOTOMY TUBE - BOBBIN WITH TAB
MYRINGOTOMY TUBE
TYMPANOSTOMY VENTILATION TUBE
TM MICRO-CATHETERS
ROUND WINDOW CATH
HOFFMAN H/A COATED LONG-TERM VENTILATION TUBE WITH LINER
ACTIVENT ANTIMICROBIAL VENTILATION TUBES
TYMPANOSTOMY VENTILATION TUBE
TYMPANOSTOMY VENTILATION TUBE
VENTILATION TUBES
MISTEN MEDICAL REUTER BOBBIN STYLE VENT TUBE
TYMPANOSTOMY TUBE
AT2 & DOYLE STYLE (C-FLEX) VENT TUBES
TYMPANOSTOMY TUBE
TYMPASNOSTOMY TUBE
TYMPANOSTOMY (VENTILATION) TUBE
TYMPANOSTOMY TUBE
COLLAR BUTTON VENTURI VENT TUBE
BOBBIN STYLE VENTURI VENT TUBE
GROMMENT STYLE VENTURI TUBE
C-FLEX VENT TUBES

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