# Oehm Und Rehbein GmbH

- Location (FDA's records): Rockstock, DE
- FDA decisions: 5 (2007–2018): 5 510(k) clearances
- Product codes: MQB (2), LLZ (2), IZL (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 15 (2 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
- 5 Star Medical, Inc.: 1 (https://510kreport.com/company/5-star-medical)
- Steinhart Medizinsysteme GmbH: 1 (https://510kreport.com/company/steinhart-medizinsysteme)
- Efilm Medical, Inc.: 1 (https://510kreport.com/company/efilm-medical)
- Sedecal., Sa.: 1 (https://510kreport.com/company/sedecal)

## Firms that cite its devices most
- Imix Adr Finland OY: 2 (https://510kreport.com/company/imix-adr-finland)
- VATECH Co., Ltd.: 1 (https://510kreport.com/company/vatech)
- Skanray Technologies Limited: 1 (https://510kreport.com/company/skanray-technologies)
- Radlink, Inc.: 1 (https://510kreport.com/company/radlink)
- Minxray, Inc.: 1 (https://510kreport.com/company/minxray)
- Imfou Co., Ltd.: 1 (https://510kreport.com/company/imfou)
- Sedecal., Sa.: 1 (https://510kreport.com/company/sedecal)
- Eponatech, LLC: 1 (https://510kreport.com/company/eponatech)

## Its most-cited devices
- K091364: Dicompacs, Model 5.2, Dicompacs DX-R, Model 1.4 (2009), cited by 5
- K070618: Dicompacs, Model 5 (2007), cited by 5
- K182317: AMADEO M-DR mini, AMADEO M-AX mini (2018), cited by 3
- K141440: Dicompacs DX-R with Flat Panel (2014), cited by 1
- K131211: Dicompacs DX-R with Flat Panel (2013), cited by 1

## Recent decisions
- K182317: AMADEO M-DR mini, AMADEO M-AX mini (Sep 24, 2018)
- K141440: Dicompacs DX-R with Flat Panel (Aug 29, 2014)
- K131211: Dicompacs DX-R with Flat Panel (Nov 5, 2013)
- K091364: Dicompacs, Model 5.2, Dicompacs DX-R, Model 1.4 (Dec 11, 2009)
- K070618: Dicompacs, Model 5 (Apr 25, 2007)

Source page: https://510kreport.com/company/oehm-und-rehbein