# Engineering, Inc.

- Location (FDA's records): Foster City, CA
- FDA decisions: 5 (1986–1988): 5 510(k) clearances
- Product codes: KDQ (1), GDM (1), DXT (1), BTA (1), HHI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 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
- Medical Device Resource Corp.: 1 (https://510kreport.com/company/medical-device-resource)

## Its most-cited devices
- K854844: LS1000 Surgical Aspirator II (1986), cited by 1

## Recent decisions
- K881521: Modified Servo Syringe (May 31, 1988)
- K862749: LS9000 Suction Biopsy Needle (Sep 15, 1986)
- K862476: LS3000 Cannula Uterine Suction (Jul 18, 1986)
- K854359: LM2000A Surgical Suction Monitor (Mar 3, 1986)
- K854844: LS1000 Surgical Aspirator II (Feb 12, 1986)

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