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Just for some background information on how most countries tend to rely on larger, more rigorous regulatory bodies...
I am in the pharma industry (not in vaccines though). Typically the two main regulators that most other countries look to as a reference are either the FDA or the EMA (the EU organization). This usually means that if you can satisfy the requirements of one of these bodies, then it is satisfactory for the other country as well. However, it isn't universal as each other country will usually have some modifications here and there for whatever reason. The most annoyingly particular ones I have dealt with in the past are China and Japan.
Hey, the NHS in the UK sometimes does things, too!
Looks like the WHO also leads vaccine strategy meetings, according to the ECDC. https://www.ecdc.europa.eu/en/seasonal-influenza/prevention-and-control/vaccines/vaccination-strategies
So I think the odds that no vaccines are available in the US are low, but I don't know if the same flu strains are targeted across the pond.