# Preceptis Medical

- Location (FDA's records): Plymouth, MN
- FDA decisions: 5 (2014–2022): 5 510(k) clearances
- Names in FDA's records: Preceptis Medical (3); Preceptis Medical, Inc. (2)
- Product codes: ETD (5)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 6 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Micromedics, Inc.: 1 (https://510kreport.com/company/micromedics)
- Heinz Kurz GmbH Medizintechnik: 1 (https://510kreport.com/company/heinz-kurz-medizintechnik)

## Firms that cite its devices most
- Aventamed Dac: 2 (https://510kreport.com/company/aventamed-dac)
- Tusker Medical, Inc.: 1 (https://510kreport.com/company/tusker-medical)

## Its most-cited devices
- K200952: Hummingbird Tympanostomy Tube System (2020), cited by 2
- K221254: Hummingbird Tympanostomy Tube System (2022), cited by 2
- K142282: Hummingbird (TM) Tympanostomy Tube System (TTS) (2015), cited by 1
- K133921: Preceptis Tympanostomy Tube Inserter (2014), cited by 1

## Recent decisions
- K221254: Hummingbird Tympanostomy Tube System (Jul 27, 2022)
- K200952: Hummingbird Tympanostomy Tube System (Jun 5, 2020)
- K151830: Hummingbird Tympanostomy Tube (Sep 21, 2015)
- K142282: Hummingbird (TM) Tympanostomy Tube System (TTS) (Apr 23, 2015)
- K133921: Preceptis Tympanostomy Tube Inserter (Aug 22, 2014)

Source page: https://510kreport.com/company/preceptis-medical