# Interlace Medical, Inc.

- Location (FDA's records): Farmingham, MA
- FDA decisions: 7 (2008–2011): 7 510(k) clearances
- Product codes: HIH (6), GCJ (1)
- Predicates its devices cite: 14 (5 its own); citations of its devices by later devices: 11 (5 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
- Smith & Nephew, Inc.: 3 (https://510kreport.com/company/smith-nephew)
- Henke Sass Wolf of America, Inc.: 2 (https://510kreport.com/company/henke-sass-wolf-of-america)
- Henke-Sass, Wolf GmbH: 1 (https://510kreport.com/company/henke-sass-wolf)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- ETHICON, Inc.: 1 (https://510kreport.com/company/ethicon)
- Lumenis, Inc.: 1 (https://510kreport.com/company/lumenis)

## Firms that cite its devices most
- Hologic, Inc.: 6 (https://510kreport.com/company/hologic)

## Its most-cited devices
- K100559: Myosure Hysteroscopic Tissue Removal System (2010), cited by 5
- K091465: Myosure Rod Lens Hysteroscope (2009), cited by 3
- K091100: Myosure Hysteroscopic Tissue Removal System (2009), cited by 2
- K073690: Interlace Medical Hysteroscopic Morcellation System (2008), cited by 1

## Recent decisions
- K103741: Surgisure Tissue Removal System (Mar 2, 2011)
- K102686: Myosure Rod Lens Scope Seals (Oct 15, 2010)
- K100559: Myosure Hysteroscopic Tissue Removal System (Mar 30, 2010)
- K091100: Myosure Hysteroscopic Tissue Removal System (Oct 23, 2009)
- K091465: Myosure Rod Lens Hysteroscope (Aug 21, 2009)
- K081070: Interlace Medical Operative Hysteroscopy System (Jul 23, 2008)
- K073690: Interlace Medical Hysteroscopic Morcellation System (Apr 17, 2008)

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