Disposable ear curettes are single-use tools designed to help remove ear wax, also known as cerumen. This American Hospital Supply guide helps you compare ear curette sizes, tip styles, and options for adults, children, and infants so you can select the appropriate ear wax removal tool for different needs.
Choose an ear curette tip based on the patient’s age, ear canal size, and the type and consistency of the earwax. Use the general guidelines below to help select the appropriate curette.
4mm Blue Spoon Tip
For Adults
Scoop and remove soft earwax from adult and adolescent ear canals.
2mm Gray Spoon Tip
For Infants
Safely clear soft earwax from a baby’s ear canal.
4mm Green Round Tip
For Adults
Safely remove earwax and debris from the ear canal.
3mm Pink Round Tip
For Adults or Pediatric
Safely remove harder earwax from pediatric or adults ear canals.
4mm White Oval Tip
Universal
General-purpose earwax removal and normal curettage.
Variety Pack
For All
Includes five color-coded tip styles and sizes for pediatric and adult earwax removal.
How to Use
- Position the patient comfortably.
Seat the patient on an examination table or stable chair and ask them to remain still during the procedure. - Examine the ear canal first.
Use an otoscope to locate the cerumen (earwax) and identify the position of the tympanic membrane (eardrum) before inserting the curette. - Straighten the ear canal.
Gently pull the outer ear up and back to help straighten the ear canal. Carefully insert the curette, loosen the earwax, and gently draw it out of the canal. - Check the ear canal as you work.
Check the ear canal as you work. Use the otoscope periodically to check for remaining earwax. If needed, repeat the process carefully until enough cerumen has been removed to clearly examine the tympanic membrane.
Important Safety Information
- Stop use immediately if bleeding, irritation, or any injury to the ear canal or tympanic membrane or eardrum occurs.
- Single-use only. Do not reuse. Discard the curette after use.
- 510(k) exempt medical device. This product is classified as a 510(k)-exempt device under applicable FDA requirements.
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