# Intermedics, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 211 (1977–1996): 211 510(k) clearances
- Product codes: DTB (105), DXY (52), DTD (14), FRN (7), DXH (5), KRG (4), GZJ (3), GEI (2), DTE (2), DTR (1), HPS (1), HLM (1)
- Predicates its devices cite: 24 (24 its own); citations of its devices by later devices: 26 (24 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Micrel Medical Devices S.A.: 1 (https://510kreport.com/company/micrel-medical-devices)
- Biotronik, Inc.: 1 (https://510kreport.com/company/biotronik)

## Its most-cited devices
- K902672: Intermedics 430-07 Bipol Implant Endocard Pac Lead (1991), cited by 4
- K954719: Intermedics Model 430-07 Bipolar Implantable Endocardial Pacing Lead (1996), cited by 3
- K883602: Biopore VS.1 Endocardial Inter Implant Pacing Lead (1988), cited by 3
- K922972: Models 438-05 and 435-05 Implantable Pacing Lead (1993), cited by 3
- K912235: Models 432-03 & 433-03 Implant Endocard Pac Lead (1991), cited by 2
- K890411: Models 432-03 & 433-03 Implantable Pacing Leads (1989), cited by 2

## Recent decisions
- K954610: Model 430-07 Endocardial Pacing Lead (Dec 16, 1996)
- K955122: Intermedics Model 436-07 Bipolar & Model 437-07 Unipolar Implantable Endocardial Pacing Lead (Nov 4, 1996)
- K962174: Biplr IM EN Pac Leads (430-07,432-03,436-02 & 07, 438-05 & 07) (Aug 21, 1996)
- K955550: Cardifix EZ Bipolar/Unipolar Endocardial Pacing Lead (Jun 19, 1996)
- K960281: Implantable Pacing Leads/Implantable Accessory/Non-Implantable Accessory (Jun 18, 1996)
- K954719: Intermedics Model 430-07 Bipolar Implantable Endocardial Pacing Lead (Feb 27, 1996)
- K933278: Intermedics Triangle Chest Probe Model 526-04 (Mar 15, 1995)
- K922042: Cardifix  Endocardial Pacing Lead (Apr 29, 1993)

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