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Cellfina System Cart
Model Rev R · Ulthera, Inc. · DI 00840763101015
OUP — Powered Surgical Instrument For Improvement In The Appearance Of Cellulite · Class II · 21 CFR 878.4790
UDILibrary device dossier · generated 2026-09-14 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (1)
Initiated
Recall #
Class
Status
Reason
Link basis
2016-11-14
Z-0749-2017
Class II
Terminated
It was discovered that a non-sterile vacuum tube is supplied within the pack, although the Instructions for Use (IFU) describe the use of a sterile vacuum tube as part of the procedure setup.
k number procode
Adverse-event reports — MAUDE (0)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-05
0
2
2019-07
0
1
2021-12
0
1
2022-06
0
4
2022-07
0
4
2022-09
0
1.5
2022-10
0
3
2022-12
0
1
2023-01
0
2
2023-03
0
1
2023-04
0
1
2023-06
0
1
2023-07
0
3
2023-08
0
1
2023-09
0
1
2023-11
0
1
2024-01
0
1
2024-04
0
2
2024-10
0
1
2024-11
0
1
2025-04
0
1
2025-05
0
2
2025-08
0
1
This device (reports/month)Average device in OUP (reports/device/month)
Regulatory clearances
K161885 SESE 2016-10-05 (k number procode)
Predicate lineage
K161885 — cites (transitively): K153677 (d1), K150505 (d2), K101231 (d3), K134010 (d3) — cited as predicate by K192185
Lineage extracted from public 510(k) summary text (heuristic).