# Instrumentarium Corp.

- Location (FDA's records): Milwaukee, WI
- FDA decisions: 20 (1983–2002): 20 510(k) clearances
- Product codes: EHD (4), LNH (4), MUH (2), CCK (2), IZH (2), CBQ (1), FFT (1), DRT (1), CCJ (1), DPS (1), JJS (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 13 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Instrumentarium Corp. Imaging Division: 3 (https://510kreport.com/company/instrumentarium-imaging-division)
- J. Morita USA, Inc.: 2 (https://510kreport.com/company/j-morita-usa)
- J. Morita Mfg. Corp.: 2 (https://510kreport.com/company/j-morita-mfg)
- VATECH Co., Ltd.: 1 (https://510kreport.com/company/vatech)
- Optical Sensors, Inc.: 1 (https://510kreport.com/company/optical-sensors)
- Hdx Will Corp.: 1 (https://510kreport.com/company/hdx-will)
- Datex-Ohmeda, Inc.: 1 (https://510kreport.com/company/datex-ohmeda)
- Midmark Corp.: 1 (https://510kreport.com/company/midmark)

## Its most-cited devices
- K001439: Orthoceph OC100 D (2000), cited by 4
- K992385: Orthopantomograph OP100D (1999), cited by 3
- K930338: Orthoceph OC100 (1993), cited by 2
- K962638: Tonocap, TC-200 and Accessory Catheters (1997), cited by 2
- K001729: FOCUS (2000), cited by 1
- K934478: Alpha Stereo (1995), cited by 1

## Recent decisions
- K022630: Modification to Focus (Oct 9, 2002)
- K001729: FOCUS (Jul 13, 2000)
- K001439: Orthoceph OC100 D (Jun 22, 2000)
- K992385: Orthopantomograph OP100D (Sep 28, 1999)
- K981641: Mammography X-Ray Equipment Models MGF101 and MGF110, Alpha Iii, Alpha ST, Alpha RT and Alpha IQ (Jul 17, 1998)
- K962638: Tonocap, TC-200 and Accessory Catheters (Apr 4, 1997)
- K961441: Tonometered Slaine Blood Gas Control (Apr 30, 1996)
- K955018: Trip NGS & Sigmoid Catheter Phi Slide Calculator (Jan 30, 1996)

Source page: https://510kreport.com/company/instrumentarium