# Aesthetech Corp.

- Location (FDA's records): Paso Robles, CA
- FDA decisions: 6 (1981–1987): 6 510(k) clearances
- Product codes: LZK (1), LCJ (1), HQC (1), FWP (1), BTA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K873940: Creat Brand O-Rise General Aspirator (Nov 25, 1987)
- K873434: Creat Brand Malar Implant (Sep 11, 1987)
- K853189: Creat Brand I/a Pack Creat Brand Phaco Pack (Sep 24, 1985)
- K843678: Creat Brand Skin Expander (Nov 6, 1984)
- K841283: Disposable Suction Tubing Set (Apr 24, 1984)
- K812210: Creat Brand Wagner Chin Implant (Sep 11, 1981)

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