MI
Movano Inc. (MOVE)·Q3 2024 Earnings Summary
Executive Summary
- Q3 revenue was $0.05M, with 339 Evie Rings shipped, as the team executed a September 17 back‑in‑stock relaunch; operating loss narrowed year over year to $(7.4)M from $(9.1)M, and net loss to $(7.2)M from $(9.0)M .
- Management emphasized strong D2C execution (90%+ customer service approval), an organic go‑to‑market into the holidays, and the imminent launch of the Android app to expand TAM; B2B pipeline advanced with an agreement‑phase pilot in Q1 2025 pending EvieMED clearance .
- The company submitted its complete response to the FDA during the week of Oct 28 and remained in the final stage of EvieMED 510(k) review through Q3; subsequent to quarter‑end (Dec 2), Movano received FDA clearance for EvieMED’s pulse oximeter, a major B2B catalyst .
- Corporate actions: 1‑for‑15 reverse split (Oct 29) regained NASDAQ bid‑price compliance (Nov 12); management disclosed an investigation into apparent stock manipulation of single‑share transactions around the split .
What Went Well and What Went Wrong
What Went Well
- D2C relaunch traction with improved experience and operations; management cited “laser focused” execution, upcoming Android app, and holiday campaigns, with 90%+ customer service approval scores .
- B2B commercialization progressed: agreement phase with a large healthcare company for a Q1 2025 pilot; re‑engagement with pharma, CROs, payors across clinical trials, RPM, and metabolic solutions ahead of clearance .
- R&D momentum: completed a UCSF hypoxia clinical trial with an updated wrist wearable featuring 12 additional mmWave antennas and enhanced multi‑analyte monitoring (SpO2, respiration, ECG), aiming to ease placement sensitivity and improve data collection .
What Went Wrong
- Minimal Q3 revenue ($0.05M) and low shipment volumes (339 rings) as the relaunch occurred late in the quarter; sequential operating loss increased to $(7.4)M versus Q2 $(6.4)M, with cash burn ~$5.6M in Q3 (including ~$1M one‑time/annual payments) .
- Q2 revenue was effectively zero due to prior deferred revenue offsets and refunds from initial launch issues; this dampened sequential revenue trajectory despite Q1’s $0.85M .
- No quantitative guidance (revenue/margins/OpEx) provided; visibility on near‑term financial trajectory remained limited pending scale‑up of D2C marketing, Android launch, and EvieMED B2B ramp .
Financial Results
Year-over-year comparison:
Notes:
- EPS comparability is affected by the 1‑for‑15 reverse split implemented Oct 29, 2024; Movano regained NASDAQ bid‑price compliance on Nov 12, 2024 .
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “We are pleased with our Evie Ring D2C performance and continue to be laser focused on improving the consumer experience, including the upcoming launch of our Android app… Additionally, we look forward to the successful completion of the 510(k)… and… game changing opportunities… for our healthcare partners.” — CEO John Mastrototaro .
- “We shipped 339 rings in the stub period of the third quarter… focus… on a fully organic basis without marketing dollars… plenty of inventory on hand… cash burn… ~$5.6M including ~$1M one‑time payments.” — CFO Jeremy Cogan .
- “Our updated device features 12 additional millimeter wave antennas… delivers enhanced data collection with less impact of placement… monitors pulse rate, SpO2, respiration rate and ECG waveforms.” — CEO John Mastrototaro on cuffless BP wearable .
- “The AI‑powered [insights] engine is getting smarter every day… discovering new ways to correlate the data… to help… improve overall health.” — CMO Tyla Bucher .
Q&A Highlights
- Cuffless blood pressure roadmap: Management expects accuracy at least on par with prior FDA‑criteria study; ongoing iterations to slim form factor and multiple trials planned over the next year .
- Android parity and TAM: Android app will have full feature parity with iOS; ~40% of prospective users are Android; expected demand bump on launch .
- OpEx and cash burn: Incremental spend anticipated for holidays/Android, but overall continued discipline in resource management and burn reduction focus .
- FDA process clarity: Final stage focused on medical aspects (including labeling); strong clinical evidence with superior accuracy to hospital pulse oximeters; waiting for remaining agency feedback by Q3 end .
Estimates Context
- S&P Global consensus EPS and revenue estimates for Q3 2024 were unavailable at the time of analysis due to an access limit; as a result, no vs‑consensus comparisons can be provided for this quarter [SPGI access error via GetEstimates].
- Given the subsequent FDA clearance (Dec 2), we expect analysts to update B2B revenue trajectories and timing assumptions around pilots and initial deployments in 2025 .
Key Takeaways for Investors
- Near‑term D2C: Expect holiday season and Android launch to drive improved top‑line versus Q3’s stub; watch conversion efficiency as the team shifts from organic to measured paid spend .
- B2B inflection: FDA clearance (post‑period) materially de‑risks B2B use cases (clinical trials, RPM, payor pilots); pipeline already at agreement phase with pilots slated for early 2025—monitor contract formalization and deployment velocity .
- R&D optionality: Continued advancement in cuffless BP/glucose with proprietary RF SoC and improved antenna arrays creates long‑term upside if accuracy and regulatory milestones are achieved; near‑term path involves more trials and hardware iteration .
- Financial discipline: Q3 burn of ~$5.6M (incl. ~$1M one‑time) shows continued resource focus; cash of $11.3M at quarter‑end provides a runway for holiday D2C and initial B2B onboarding—investors should watch burn and gross margin trends as volumes scale .
- Corporate housekeeping: Reverse split and regained NASDAQ compliance remove listing overhang; ongoing investigation into apparent manipulation indicates proactive governance posture .
- Narrative shift: With clearance in hand, the story pivots from product readiness to commercialization—KPIs to track: signed B2B agreements, pilot start dates, active patients/devices, and D2C unit momentum post‑Android .
- Risk‑reward: Execution risk remains on scaling production, maintaining quality/CSAT, and meeting data/compliance needs for partners; clearance and pipeline breadth provide visible catalysts, but revenue ramp timing should be managed conservatively .
KPIs (Operational and Balance Sheet)
Segment Breakdown
- Not applicable; the company reports as a single operating entity with D2C shipments disclosed and B2B pipeline commentary; no segment financials provided for Q3 2024 .
Disclosures and Subsequent Events
- FDA 510(k) clearance for EvieMED Ring received Dec 2, 2024, unlocking B2B opportunities across clinical trials, RPM, and payor pilots; this is a key catalyst beyond Q3 .
- 1‑for‑15 reverse split (Oct 29) achieved NASDAQ bid‑price compliance (Nov 12); apparent single‑share transaction activity investigated by management .
Sources: Q3 2024 8‑K press release and financial tables ; Q3 2024 earnings call transcript ; Q2 press release and call ; Q1 press release and call ; Back‑in‑stock and FDA review updates ; Post‑period FDA clearance .