Tissue Technologies, Inc.
Tissue Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2000.
Top product codes for Tissue Technologies, Inc.
Recent clearances by Tissue Technologies, Inc.
- K002071 — SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR STRANDS AND SUTURE HOLES
- K000849 — SOFTFORM FACIAL IMPLANT
- K982475 — SOFT TISSUE AUGMENTATION YUBE WITH INSERTION TOOL
- K973462 — SOFTFORM FACIAL IMPLANT
- K970804 — TRU-PULSE CO2 SURGICAL LASER
- K963683 — TRU-PULSE LASER (MODIFIED)
- K962496 — SOFT TISSUE AUGMENTATION TUBE (S.T.A.T.)
- K960481 — SOFT TISSUE AUGMENTATION TUBE
- K952049 — TRU-PULSE PULSED CO2 SURGICAL LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.